Chronic hepatitis C: future treatment

Abstract

The launch of first-generation protease inhibitors (PIs) is a major step forward in HCV treatment. However, the major advance is up to now restricted to genotype 1 (GT-1) patients. The development of second-wave and second-generation PIs yields higher antiviral potency through plurigenotypic activity, more convenient daily administration, fewer side effects and, for the second-generation PIs, potential activity against resistance-associated variants. NS5B inhibitors include nucleoside/nucleotide inhibitors (NIs) and non-nucleotide inhibitors (NNIs). NIs have high efficacy across all genotypes. Sofosbuvir has highly potent antiviral activity across all genotypes in association with pegylated interferon and ribavirin (PR), thus allowing shortened treatment duration. NS5A inhibitors (NS5A.I) have highly potent antiviral activity. It has recently been shown for the first time that NS5A.I in combination with protease inhibitors can cure GT-1b null responders in an interferon-free regimen. Besides, several studies demonstrate that interferon (IFN)-free regimens with direct-acting antiviral agent combinations are able to cure a large number of either naïve or treatment-experienced GT-1 patients. Moreover, quadruple regimen with PR is able to cure almost all GT-1 null responders. The development of pan-genotypic direct-acting antiviral agents (NIs or NS5A.I) allows new combinations with or without PR that increase the rate of sustained virological response for all patients, even for those with cirrhosis and independently of the genotype. Therefore, the near future of HCV treatment looks promising. The purpose of this article is to provide an overview of the clinical results recently reported for HCV treatment.

Introduction

Approximately 170–200 million people worldwide (3% of the world population) are chronically infected with the hepatitis C virus (HCV).1 HCV prevalence and genotype distribution vary around the world. Among the six identified HCV genotypes, genotype 1 (GT-1) is the most prevalent worldwide; it was the most difficult to cure with the standard of care treatment: the combination of pegylated interferon (PEG-INF) alpha and ribavirin (RBV).

Chronic hepatitis C can lead to cirrhosis and subsequent complications such as hepatocellular carcinoma (HCC). Every year, more than 350,000 people woldwide die from hepatitis C-related liver diseases. The goal of HCV treatment is to achieve a sustained virological response (SVR), which is defined as undetectable HCV RNA, 6 months after cessation of therapy, leading to HCV clearance. SVR is associated with an improved histological outcome, and a reduction of morbidity and mortality.

In 2011, the launch of the two first-generation protease inhibitors (PIs), boceprevir and telaprevir, was a major step forward for the treatment of GT-1–infected patients. Associated with PEG-INF/RBV therapy (PR), these two drugs increase the chance of cure for naïve patients by 30%.2–4 The benefit is even greater in treatment-experienced patients: the chance of cure increases by 50%–60% for relapsers, 40%–45% for partial responders, and 25% for null responders.5,6 However, only GT-1 patients benefit from this major advance. For the 50–70 million people infected with other HCV genotypes, the combination of PR remains the current standard-of-care (SOC) treatment.7 The development of more effective treatments for non-GT-1 patients is essential, especially for GT-4 patients for whom SVR rates are relatively low with PR.

Different potential therapeutic targets in HCV life cycle have been identified. This has led to the development of both direct antiviral agents (DAA) and agents targeting the host functions, which are essential for viral replication. Besides the first-generation PIs boceprevir and telaprevir, DAA comprise second-wave and second-generation PIs, nucleos(t)-ide (NI) and non-nucleoside (NNI) inhibitors of the NS5B complex, and NS5A-inhibitors (NS5A.I). Host-targeting agents (HTA) are, for example, cyclophilin inhibitors and silibinin. Next-generation DAAs appear to be promising; they may enable interferon-free (INF-free) regimens for cirrhotic patients and even for patients with more advanced or decompensated cirrhosis.

The purpose of this article is to provide an overview of the recent clinical results concerning future HCV treatment of GT-1, non-GT-1, and cirrhotic patients.

Treatment of GT-1 patients beyond boceprevir and telaprevir

Triple therapy including boceprevir or telaprevir in combination with PR increases the SVR rates by 30% for naïve patients, and even more for treatment-experienced patients. However, this benefit is associated with the increase of side effects such as anemia and with the onset of new side effects: dysgeusia (nearly one-third of the patients treated with boceprevir) and cutaneous rash (55% of the patients treated with telaprevir).8 Moreover, the triple regimen results in the increase of treatment withdrawals due to adverse events. Concerning anemia management, these new treatments have led to a new paradigm: for noncirrhotic patients, the ribavirin dose can be reduced without impairing SVR, even at early stages of treatment when HCV RNA is still detectable.9–11

Second-wave and second-generation PIs

The main weaknesses of the first-generation PIs are their low genetic barrier to resistance and the fact that their effectiveness is limited to GT-1 patients. Second-wave PIs have a higher barrier to resistance, better activity against multiple genotypes except GT-3, more convenient dosing schedules, and improved safety and tolerance.12–14 Second-generation PIs are compounds that are broadly active against all genotypes and against viral isolates which carry resistance mutations for first-generation PIs.15–26 In combination with PR, the new PIs appear to achieve greater SVR rates than the first-generation PIs. These new treatments allow for more convenient administration schedules (one or two administrations per day); this could result in improved pharmacokinetics and better patient compliance. Besides, the safety profile seems to be good. The pan-genotypic activity of this new treatment provides new therapeutic options for a greater number of patients, in particular for those infected with GT-4.25,27–29

See Table 1 for an overview of the efficacy and the tolerance of the second-wave PIs, which are currently developed. Second-generation PIs are in early stage of development. MK-5172 in monotherapy demonstrates pan-genotypic activity;29 other molecules such as ACH-2684, AVL-181, and AVL-192 show promising results in vitro.30

Table 1.

Overview of clinical efficacy of second-wave PIs

Protease Inhibitor (PI)	Company	Current Clinical Phase	Number of patients	Dose Per Day	Duration of Therapy	Viral Response	Side Effects	Active against HCV Genotype
Simeprevir TMC-43515,16,96–98	Tibotec	II	461	150 mg QD	PI + PR 12–24–48 w +PR 24–36	Null-R G1: SVR: 51% Relapsers G1: SVR: 85% Partial R G1: SVR: 75%	Anemia 20% Bilirubin increase	1,2,4,5,6
		III	394 48 cirrhotic		QUEST-1: PI + PR 12 w +PR 12–36W (RGT)	Naïve G1: SVR: 80% Cirrhosis naïve GT-1 SVR12: 58%
		III	391 32 cirrhotic		QUEST-2: PI + PR 12 w +PR 12–36W (RGT)	Naïve G1: SVR: 81% Cirrhosis naïve GT1: SVR12: 65%
Faldaprevir BI-201 13517,18	Boehringer	III	656	120 mg vs 240	PI 12/24 w + 24/48 w PR	Naïve GT1: SVR: 80%	Rash; jaundice	1,2
	Ingelheim	II	288	240 mg QD	PI + PR 24 w ± 24 w PR	Null-R G1: SVR: 35% Partial R G1: SVR: 50%
Danoprevir ITMN-191, RG 722719,20	Roche	II	421	DAUPHINE: 200/r mg BID 100/r mg BID	PI/r + PR 24 w	Naïve G1: SVR24: 89% 79% 66%	Nausea, diarrhea, neutropenia ALT increase	1,2,4
			29	50/r mg BID		G4: SVR12: 100%
			49	100/r mg BID	PI/r + PR 24 w	Partial R: SVR 12: 56% G1b 91%, G1a 30%
Vaniprevira MK-700921,22	Merck	II/III	94	Naïve: 300 mg BID 600 mg BID 600 mg QD 800 mg QD	4w/44 PR	Naïve G1: SVR 61% SVR 80% SVR 78% SVR 84%	Nausea	1,2
			211	Treatment-experienced: 600 mg BID 24 w 600 mg BID 24 w + 24 w PR 600 mg BID 48 w 300 mg BID 48 w	PI + PR 24 w ± PR 24 PI + PR 48 w	Trt-experienced Null-R SVR: 71% SVR: 50% SVR: 85% SVR: 80% SVR: 67% SVR: 50% SVR: 78% SVR: 40%
ABT-45023	Abbott	II	35	100/r or 200/r mg QD	PI + PR 12 w + 12–36 w PR	Naïve G1: SVR12: 88%	AE profile similar to PR	1
Sovaprevir ACH-162524	Achillion	II	64	200–800 mg QD	PI + PR 28 d + PR 44 w	Naïve G1: SVR12: 63–86%	AE profile similar to PR	1
			58		PI + PR 12 w + 36 PR w	Naïve G1: EOT: 69–100%
Asunaprevir BMS-65003225,26	BMS	II	47	200–600 mg BID 600 mg BID + Daclatasvir 60 mg QD ± PR 24 w	PI + PR48 w PI + NS5A inhibitor 24 w PI + NS5A inhibitor + PR 24 w	Naïve G1: SVR: 83–92% Null-R G1: SVR: 36% SVR: 100%	AE profile similar to PR	1,4

Abbreviations: AE, adverse event; BID, twice daily; EOT, end of treatment response; HCV, hepatitis C virus; PI, protease inhibitor; PI/r, ritonavir-boosted protease inhibitor; PR, pegylated–interferon + ribavirin; QD, once daily; RBV, ribavirin; RGT, response-guided therapy; RVR, rapid virologic response (Week 4); SVR, sustained virologic response; SVR12, sustained virologic response at week 12; SVR24, sustained virological response at week 24; w, week; /r, ritonavir-boosted; vs, versus.

NS5B polymerase-inhibitors (NS5B.I)

NS5B nucleoside/nucleotide inhibitors (NIs)

NIs mimic natural polymerase substrates and bind to NS5B active sites, thereby causing chain termination and increasing the number of errors when incorporated into a growing RNA chain. As these NS5B sites are well conserved among genotypes, NIs tend to have activity across all genotypes.31 They also have the highest barrier to resistance of all DAAs so far.

The first NI developed was the nucleoside analog mericitabine. In triple regimen with PR, mericitabine shows less antiviral activity for GT-1 patients compared to triple regimen with PIs.32,33 However, it has high antiviral activity for GT-2 and GT-3 treatment-experienced patients and for GT-4 patients34 (Table 2). If included in the INF-free regimen with ritonavir-boosted danoprevir and ribavirin for treatment-experienced GT-1b patients, or in quadruple therapy with boosted danoprevir and PR for treatment-experienced GT-1 patients, mericitabine leads to promising SVR rates20 (Table 3).

Table 2.

Overview of clinical efficacy of NS5B NIs or NNIs polymerase inhibitors

Polymerase inhibitors	Company	Current clinical phase	Number of patients	Dose per day	Duration of therapy	Viral response	Side effects	Active against HCV genotype
Nucleoside or nucleotide inhibitors
RG-7128 Mericitabine32–34	Roche	II	408	1000 mg BID	NIs + PR 12 w + PR 12/36 w RGT	Naïve: SVR24 G1/G4: 33%–51%	AE profile similar to PR	1,4
		II	166	1000 mg BID	NIs + PR 24 w ± PR 24 w RGT	Naïve SVR 24: 57%		1,4
		II	25	1500 mg BID	NIs + PR 4 w + PR 20/40 w RGT	Relapsers G2/3 SVR: 70% Null responders G2/3 SVR: 60%		2,3
GS-7977 Sofosbuvir35–39, 99–105	Gilead	II	25	400 mg QD	NIs + PR 12 w	Naïve SVR 12: 100%	AE profile similar to PR	2,3
		II	95	ELECTRON 400 mg QD	NIs + RBV 12 w + PR (4,8,12 w in total) INF-free: NIs + RBV 12 w	Naïve GT2,3 SVR 12: 100% Naïve GT1: SVR: 84% Null-R GT1: SVR4: 11%		2,3 1,2,3
			34		INF-free : NI+NS5A.I (LDV)+RBV 12w	Naïve GT1: SVR12: 100% Null-R GT1: SVR12: 100%
			35		INF-free : NI+NNI (GS 9669) +RBV 12w	Naïve GT1: SVR12: 92% Null-R GT1: SVR12: 100%
			71		NIs + PR 12 w + PR (12/36 w)	Naïve GT1: SVR 12: 88%–91%
		II	332	PROTON 200–400 mg QD	NIs + PR 12 w ±NI 12 w or NI + RBV 12 w	Naïve GT1: SVR24 : 87–89%		1
		II			NI + PR 24 w	Naïve GT4,6 SVR24: 82%, 100%
			34	ATOMIC	INF-free:NIs + LDV + RBV 12 w	Naïve GT1: SVR12: 100%		1,4,6
		II		400mg QD		Naïve GT1: SVR12: 100%
		III	327	NEUTRINO 400mg QD	NI+PR 12w	Naïve GT1,4,5,6: SVR12: 90%; cirrhosis 80%
Non nucleoside inhibitors
NNI-Site 1 inhibitors BI 207 12740			400 mg TID 600 mg TID 800 mg TID		NNIs + PR 28 days + PR 40 w	Naïve G1: RVR: 50% RVR: 57% RVR: 50%
		II	57			Trt-experienced G1	Nausea, vomiting, diarrhea, rash	1
	Bohringer Ingelheim			400 mg TID 600 mg TID 800 mg TID		RVR: 0% RVR: 22% RVR: 18%
NNI-Site 2 inhibitors Filibuvir41	Pfizer	II	35	200 mg BID300 mg BID 500 mg BID	NNIs + PR 28 day + PR 44 w	Naïve G1 RVR: 60% SVR12: 30% RVR: 75% SVR12: 50% RVR: 63% SVR12: 50%	Nausea asthenia	1
NNI-Site 2 inhibitorsVX-22242	Vertex	I	24	250 mg BID 500 mg BID 750 mg BID 1500 mg QD	NNIs 3 days	Mean HCV RNA reduction −3.2 log 10 IU/ml	Diarrhea (25%) Headache (20%) Nausea (12%)	1
NNI-Site 3 inhibitors Setrobuvir ANA59843	Anadys	II	60	200 mg BID 400 mg BID	NNIs + PR 12 w + PR 24/36 w	Naïve G1: RVR: 56% EVR: 73% RVR: 42% EVR: 75%	Rash	1
NNI-Site 3 inhibitors ABT-33344	Abbott	II	16	400 mg BID 800 mg BID	NNIs 2 days + PR 12 w + PR 36 w	Naïve G1 SVR24: 63% SVR24: 63%	AE profile similar to PR	1
NNI-Site 3 inhibitors ABT-07244	Abbott	II	23	100 mg QD 300 mg QD 600 mg QD	NNIs + PR 12 w + PR 36 w	Naïve G1: SVR24: 50% SVR24: 25% SVR24: 86%	AE profile similar to PR	1
NNI-Site 4 inhibitors Tegobuvir (GS9190)45	Gilead	II	252	40 mg BID	NNIs + PR 24 w or 48 w	Naïve SVR: 56%	Rash	1

Abbreviations: AE, adverse event; EVR, early virologic response (Week 12); BID, twice daily; HCV, hepatitis C virus; NI, nucleotide inhibitor; NNI, non-nucleoside inhibitor; PR, pegylated–interferon + ribavirin; RBV, ribavirin; RGT, response-guided therapy; QD, once daily; RVR, rapid virologic response (Week 4); SVR, sustained virologic response; SVR12, sustained virologic response at week 12; w, week.

Table 3.

Overview of clinical efficacy of DAAs combination studies

Combination trials	Company	Current clinical phase	Number of patients	Dose per day	Duration of therapy	Viral response	Active against HCV genotype
PI and NS5B NIs
Danoprevir and mericitabine20,61,62	Roche			INFORM -1
		I	64	Danoprevir + Mericitabine 900 mg BID + 1000 mg BID	14 days then PR 48 W	Naïve: EOT: 100% < LLQ Null- Rito: EOT: 66% < LLQ	1
				INFORM SVR
		II	54	Danoprevir/rito+ Mericitabine + RBV	24 w	Naïve SVR: 41% (G1b:71%, G1a:26%)	1
				MATTERHORN
			31	Danoprevir/rito+ Mericitabine + RBV	24 w	Partial R SVR: G1b: 39% Null-R SVR: G1b: 55%
			124	Or Danoprevir/rito+ Mericitabine + RBV +PEG (100 mg BID/100 mg BID + 1000 mg BID)	24 w	Partial R: G1b: 96%/G1a:75% Null-R: G1b: 100%/G1a: 73%	1
TMC-435 + GS -7977 Simeprevir and Sofosbuvir95,106	Tibotec Gilead	II	80	Simeprevir + Sofosbuvir ± RBV 150 mg QD + 400 mg QD	PI + NIs 12 w or 24 w PI + NIs + RBV 12 w or 24 w	Null –R G1 SVR12: 93%	1
PI and NS5B NNIs
BI 201335 (Faldaprevir) + BI	Bohringer			SOUND-C2
207127-(Deleobuvir)63–65	Ingelheim	IIb	362	Faldaprevir + BI 207127 + RBV 120 mg QD + 400/600 mg TID	PI + NNIs + RBV 16 w 28 w or 48 w	Naïve: SVR12: G1b 55%–84%, G1a 38%–47%	1 1
Telaprevir + VX-22265,66	Vertex	II		ZENITH
			5,6	Telaprevir + VX-222+ RBV 1125 mg BID + 100/400 mg BID or	PI + NNIs + RBV 12 w	Naïve: SVR: G1b: 70%, G1a: 73%	1
			13,14	Telparevir + VX 222 + PR 1125 mg BID + 100/400 mg BID	PI + NNIs + PR 12 w + PR 12 w	Naïve: SVR12: 83%–90%
GS 9256 + GS9190 (Tegobuvir)68	Gilead	II	42	GS 9256 + Tegobuvir 75 mg BID + 40 mg BID	PI + NNIs 4 w + PR 44 w PI + NNIs + RBV 4 w + PR 44 w PI + NNIs + PR 4 w + PR 44 w	Naïve G1: RVR: 7% RVR: 38% RVR: 100%	1
ABT-450/rito + ABT-33369,70	Abbott	II	50	ABT-450/rito + ABT-333 + RBV Naïve GT1:250/100 mg or 150/100 mg BID + 400 mg BID Null-R GT1: 150/100 mg BID + 400 mg BID	PI/r + NNIs 12 w	Naïve G1 SVR12: 93%–95% Null-R G1 SVR12: 47%	1
			40	Naïve GT1: 150/100 mg BID + 400 mg BID		Naïve GT1 SVR12: 85,4%
ABT-450/rito + ABT-07271	Abbott	II	11	ABT-450/rito + ABT-072 +RBV	PI/r + NNIs +RBV 12 w	Naïve G1 ILB28CC SVR 24: 91%	1
PI and NS5A Inhibitor
BMS-650032 + BMS-790052 (Asunaprevir + Daclatasvir)26, 50,72	BMS	II	21	Asunaprevir + Daclatasvir ± PR 200 mg BID + 60 mg QD	PI + NS5A ± PR 24 w	Null-R: SVR24: 91% Intolerants: SVR: 64%	1b
			38	Asunaprevir + Daclatasvir 24 w 200 QD or BID + 60 mg	PI+ NS5A 24 w	Null-R: SVR12: 65%–78%	1b
			41	Asunaprevir + Daclatasvir + PR24 w 200 QD or BID + 60 mg	PI + NS5A + PR 24w	Null-R: SVR 4: 90%–95% GT-1a: 88%	1
ABT-450/rito + ABT26770	Abbott	II	124	ABT-450/rito + ABT-267 + RBV	PI + NS5A + RBV 12 w	Naïve GT1 SVR12: 87.3% Null-R GT1 SVR12: 89%	1
GS-9451+ GS-5885(Ledipasvir)107–109	Gilead	II	244	GS-9451 + GS-5885 + PR 200 mg QD + 30 mg QD + PR	6 w or 12 w	Naïve GT-1 IL28BCC : SVR 12 (6w) :79% SVR 12 (12w) : 98%
			348	Versus PR	12 or 24 w according to RVR	Naïve GT-1 : SVR 12 : 84%
			163		24 or 48 w according to RVR	TE GT-1 non cirrhotic : SVR 12 : 70%
NS5A Inhibitor + NS5B NIs
BMS-790052 + GS-7977 (Daclatasvir + Sofosbuvir)51,73,110,111	BMS Pharmasset	II	88 (44 GT1, 44 GT2,3)	Daclatasvir + Sofosbuvir ± RBV 60 mg QD + 400 mg QD	24 w	Naïve G2,3: SVR24: 88–100% Naïve G1: SVR24: 93–100%	1, 2, 3
			41 TE GT-1 PI-failure		24 w	TE, PI-failure GT-1 non cirrhotic : SVR12 : 100%	1
PI + NS5A Inhibitor + NS5B NNIs
BMS-650032 (Asunaprevir) + BMS-791325+ BMS-790052 (Daclatasvir)74	BMS	II	32	Asunaprevir + BMS-791325 + Daclatasvir	12 w or 24 w	Naïve G1 SVR4: 94% (GT1a: 92–100%)	1
ABT-450/rito+ ABT-333 + ABT-26770	Abbott	II	80	ABT-450/R + ABT-333 + ABT-267 + RBV	8 w	Naïve GT1 SVR12: 87,5%	1
			124	ABT-450/R + ABT-333 + ABT-267 + RBV	12 w	Naïve GT1 SVR12: 99% Null-R GT1 SVR12: 93%
			70	ABT-450/R + ABT-333 + ABT-267	12 w	Naïve GT1 SVR12: 87%
GS-9451 + GS-5885 + Tegobuvir52,53,92–94	Gilead	II	94	GS-9451 + GS-5885 ± tegobuvir ± RBV	12 w or 24 w	Naïve GT1 SVR4: 97% (GT1a 96%, GT1b 100%)	1

Abbreviations: AE, adverse events; DAA, direct antiviral agents; EVR, early virologic response (Week 12); PI, protease inhibitor; PR, pegylated–interferon + ribavirin; RBV, ribavirin; RGT, response-guided therapy; /r, ritonavir boosted; RVR, rapid virologic response (Week 4); SVR, sustained virologic response; SVR12, sustained virologic response at week 12; w, week.

The pyrimidine nucleotide analog sofosbuvir has highly potent pan-genotypic antiviral activity and a high genetic barrier to resistance. In combination with ribavirin in an INF-free regimen for 12 weeks, sofosbuvir achieves SVR rates from 84% to 100% for GT-1, GT-2, and GT-3 naïve patients. For treatment-experienced GT-1 patients, SVR rates are lower (11%); almost all patients relapse after treatment discontinuation.35,36 Triple regimen with PR for GT-1, GT-2, GT-3, GT-4, and GT-6 naïve patients achieves SVR rates from 88%–100%37–39 (Table 2). At the moment, sofosbuvir is also used in combination with PIs or NS5A.I (with or without ribavirin).

Non-nucleotide inhibitors (NNIs)

NNIs have a restricted spectrum of activity against the various genotypes, and a low barrier to resistance. They are active against GT-1, with less antiviral activity for GT-1a infected patients than for GT-1b infected patients. Table 2 gives an overview of the clinical efficacy of NNIs in combination with PR.40–45 They appear to have less antiviral activity compared to triple regimen with PIs or NS5A.I. Nevertheless, the fact that they target five different sites of the NS5B-polyprotein suggests that combinations with other NNIs or with different DAAs (PIs or NS5A.I) could be effective.

NS5A-complex-inhibitors (NS5A.I)

HCV NS5A is a phosphoprotein. It does not possess any enzymatic function, but has a crucial role in HCV replication. NS5A is comprised of three structural domains as well as an amphipathic alpha helix that functions in membrane localization. Domain I is essential for viral RNA replication. Domain II is involved in the binding to cyclophilin A. It has been postulated to play a role in antagonizing the innate immune response to HCV. Domain III seems to be important for the assembly of infectious viral particles.46 The first-in-class NS5A.I daclatasvir shows potent pan-genotypic antiviral activity. It has a low barrier to resistance. Especially GT-1a patients can select resistance-associated variants (RAVs) after a single administration.

In triple therapy with PR, daclatasvir demonstrates high antiviral potency for GT-1 and GT-4 naïve patients47 (Table 4). Studies with treatment-experienced GT-1 patients and with GT-2/3 are still ongoing.48,49

Table 4.

Overview of clinical efficacy of NS5A inhibitors

NS5A-Inhibitor	Company	Phase	Number of patients	Dose per day	Duration	Viral response	Side effects	Active against genotype
Daclatasvir (DCV) BMS-79005247–49	BMS	II	395 (G1 365, G4 30) COMMAND-1	20–60 mg QD	NS5A.I + PR 12–24 w + PR 12–36 w (max 48 w)	Naïve GT1: SVR12: 64% (G1a: 58%, G1b: 78–87%) GT4: SVR12: 100%	Nausea and dry skin	1,4
			419 COMMAND-2	20–60 mg QD	NS5AI + PR 24 w	Null-R: cEVR: 30–34% Partial R: cEVR: 44–57%		1
			151 COMMAND-GT2/3	60 mg QD	NS5A.I + PR 12 w ± PR 12 w RGT NS5A.I + PR 16 w ± PR 12 w RGT versus PR 24 w	Naïve G2: cEVR: 83–92% vs 77% Naïve G3: cEVR: 81–89% vs 59%	Profile similar to PR	2–3
ABT 26752	Abbott	II	29	5–200 mg QD	NS5A.I + PR 12 w + PR 36 w	Naïve GT1: cEVR: 80–100%	Profile similar to PR	1

Abbreviations: cEVR, complete early virologic response (Week 12); PR, pegylated–interferon + ribavirin; QD, once daily; RBV, ribavirin; RGT, response-guided therapy; RVR, rapid virologic response (Week 4); SVR, sustaines virologic response; SVR12, sustained virological response at week 12; wk, week.

Quadruple therapy with daclatasvir in association with the PI asunaprevir and PR for 24 weeks results in SVR rates of more than 90% for GT-1 null responders (who are the most difficult to treat).26,50 However, this approach is feasible only for patients who can tolerate PEG-INF and ribavirin. For cirrhotic patients, response rates are likely to be lower, while adverse event rates are probably higher.

Several INF-free regimens with daclatasvir have been studied. Dual therapy with daclatasvir and asunaprevir for 24 weeks achieves SVR for 65%–78% of GT-1b patients who are previous null responders.50 Dual or triple therapy with daclatasvir or sofosbuvir (with or without ribavirin) for 24 weeks achieves SVR for 93%–100% of naïve GT-1 patients and for 83%–100% of naïve GT-2/3 patients.51

Other NS5A.I are currently in development. In association with PR, ABT-267 shows promising on-treatment results.52 Ledipasvir has been studied in quadruple regimen, either with PI and PR or in INF-free regimen with PI, NNI, and ribavirin.53 Second-generation NS5A.I, including MK-8742 and ACH-3102, have been developed, but clinical results are pending.

Host targeting agents (HTA) and other antiviral treatments

Cyclophilins are a highly conserved family of human enzymes involved in cellular processes associated with protein folding, transport, and secretion, as well as mitochondrial function and immune response.54 HCV can coopt cyclophilins as cofactors for viral replication. In the hepatocyte, cyclophilin A and B bind with the viral proteins NS5A, NS5B, and NS2 to form a replication complex mediating the correct folding and trafficking of HCV proteins. Thus they are functioning as a positive modulator for HCV replication.55 Alisporivir (Debio 025) (ALV) is a nonimmunsuppressive form of cyclophilin inhibitor that shows a potent antiviral activity for many HCV genotypes, low resistance rates without cross-resistance to PI, NS5B.I, and NS5A.I. Phase II studies show increased SVR rates compared to PR for naïve G1 patients receiving a combination of ALV and PR for at least 24 weeks. For GT-1 treatment-experienced patients, ALV + PR demonstrated higher complete early virological response compared to PR in relapsers, partial responders, and null responders.56 Moreover, for GT-2/3 naïve patients, the possibility of an INF-free regimen has been studied.57 Among patients treated with only ALV or with RBV in combination, 22%–34% reach rapid virological response (RVR) and undergo 24 weeks of INF-free treatment. SVR in this subgroup varies from 82% to 91%. These results demonstrate the ability of such a regimen to cure these patients.57 In the Phase II program, ALV appears to have a good safety profile, with rare cases of hyperbilirubinemia. However, during the Phase III program in April 2012, the US Food and Drug Administration (FDA) placed the ALV program on a full clinical hold and, all patients discontinued therapy. This was due to a cluster of three cases of acute pancreatitis, one of them fatal, in the treatment group receiving ALV and PR. Two other cyclophilin inhibitors are currently in development (SCY-635, NIM-811). Cyclophilin inhibitors could be an important addition to DAAs in treatment combinations; they may be able to shorten and simplify therapy. They have the potential to be a cornerstone drug for an IFN-free regimen in combination with DAAs, because they have a high barrier to resistance, no cross-resistance with DAAs, and a pan-genotypic activity. ALV development is likely to move forward, but will not be used in association with PEG-INF because of the potential risk of acute pancreatitis.

Therapeutic vaccines fail to show any significant positive results yet. GI-5005 is not able to increase SVR compared to PR alone, except in a subgroup of difficult-to-treat patients. Other vaccines, such as ChronVac-C, IC41, and TG-4040, demonstrate limited antiviral activity.30,58 Polyclonal and monoclonal antibodies do not reach any endpoint in trials evaluating recurrence after liver transplantation. Toll-like receptors may enhance the host immune system against HCV; they are currently in the early development phase.

Silibinin is a flavonoid compound targeting the host cell. It is a direct inhibitor of HCV RNA-dependent RNA polymerase and a blocker of virus entry and transmission. It was recently proved to be successful in the treatment of previous PR nonresponders.59

Peg interferon lambda has the same antiviral efficacy as PEG-INF alpha, but significantly reduces side effects for GT-1 and GT-4 patients (even if they are cirrhotic).60 It may become a new alternative in combination with DAAs.

DAA combinations: the challenge of INF-free regimens

Most DAAs currently being developed for HCV treatment have been initially tested in combination with PR. The rationale of combination therapy is to increase viral potency, to decrease viral resistance, and to avoid the use of PEG-INF.

INF-related side effects remain a major problem in clinical routine. They often affect the patient’s compliance and hinder treatment in cirrhotic patients or in those with HCV-recurrence after liver transplantation. DAA combinations may permit association of molecules with different mechanism of action, different resistance profiles, and high antiviral activity.

An overview of the efficacy and tolerability of DAA combination treatments with or without PEG-INF is outlined in Table 3.20,26,50,51,53,61–74

Quadruple therapy with PEG-INF

Four studies20,26,50,75 have been reported so far. The first study (quadruple regimen, associating asunaprevir [PI], daclatasvir [NS5A.I], and PR for 24 weeks for previous GT-1 null responders) reports SVR rates over 90%. The second study by Gilead (associating a PI, a NS5A.I, and PR for treatment duration of 6 to 24 weeks for naïve GT-1 patients) is ongoing.

Two studies combining a PI, an NS5B.I, and PR for GT-1 patients have been reported. Telaprevir (PI) plus VX-222 (NNI) and PR for 12 weeks followed by 12 weeks PR leads to SVR rates of 83%–90% for GT-1 naïve patients.75 Ritonavir-boosted danoprevir (PI/r) in combination with mericitabine (NI) and PR for 24 weeks leads to SVR rates of 75%–96% for GT-1 previous partial responders and to SVR rates of 73%–100% for GT-1 previous null responders. Overall, the results of quadruple therapy with PEG-INF show SVR rates over 90% for the most difficult-to-cure patients and a reasonable safety profile.20

Two DAAs in INF-free regimens

The first proof of concept of INF-free regimens was given by the INFORM-1 study, which demonstrates that 13 days of dual therapy with danoprevir and mericitabine are able to induce a 5.1 log₁₀ IU/mL decline from baseline for naïve GT-1 patients and a 4.9 log₁₀ IU/mL decline from baseline for treatment-experienced null responders.61 A full dual therapy with asunaprevir (PI) and daclatasvir (NS5A.I) without INF for GT-1b treatment-experienced null responders for 24 weeks shows SVR12 rates from 65%–78% up to 91% (depending on the asunaprevir dosage).26,50,72 Recently, a dual therapy with daclatasvir (NS5A.I) and sofosbuvir (NI) for 24 weeks demonstrated SVR rates from 93%–100% for GT-1 naïve patients.51 Currently, a study with simeprevir and sofosbuvir for 12 or 24 weeks for GT-1 null responders is being conducted (Table 3).

Two DAAs and RBV in INF-free regimens

Four studies combine PIs, NNIs, and RBV (Table 3). The largest trial involves 362 GT-1 naïve patients. They are treated with faldaprevir (PI), BI-207127 (NNI), and RBV for 16 to 48 weeks. SVR rates range from 55% to 84% for GT-1b patients and from 38% to 47% in GT-1a patients. A second-wave ritonavir-boosted PI (ABT-450) in association with NNIs and RBV for 12 weeks can achieve SVR rates of over 90% for GT-1 naïve patients (regardless of the HCV subtype 1a or 1b). However, SVR rate was lower in GT-1 null responders. This suggests that such a combination is not optimal for this difficult-to-treat population.

The combination of ritonavir-boosted ABT-450 (PI), ABT-267 (NS5A.I), and RBV for 12 weeks increases SVR rates up to 89% for null responders.

The addition of RBV to the combination of daclatasvir (NS5A.I) and sofosbuvir (NI) for 24 weeks did not increase the SVR rate compared to dual therapy for GT-1 naïve patients.

Three DAAs with or without RBV in INF-free regimens

Three studies53,70,74 combine a second-wave PI, an NS5B.I, and an NS5A.I with or without RBV. The first study by Gilead et al on naïve GT-1 patients associates GS-9451 (second-wave PI), ledipasvir (NS5A.I) and tegobuvir (NNI) with or without RBV for 12 or 24 weeks; the SVR-rate is 97%. The second Phase II study associates asunaprevir (PI), daclatasvir (NS5A.I), and BMS-790052 (NNI) for 12 or 24 weeks for GT-1 naïve patients; the SVR rate is 94%. The third study associates a second-wave ritonavir-boosted PI (ABT-450/r), ABT-333 (NNI), ABT-267 (NS5A.I), and RBV for 12 weeks for GT-1 naïve or treatment-experienced patients; the SVR rate is 99% for GT-1 naïve patients and 93% for GT-1 null responders. The safety profiles of these regimens appear to be good.

Treatment of non-GT-1 patients

The treatment of non-GT1 patients is based on PR, which remains the SOC treatment.7 Worldwide, between 50 and 70 million individuals are chronically infected with HCV GT-2 to GT-6.76 In some countries such as Egypt, the HCV patients have almost exclusively GT-4.

In observational cohorts like the PROPHESYS-cohort, the SVR rates are 41%, 61%, 59%–68%, and 71% for GT-4, GT-3, GT-5/6, and GT-2 patients, respectively.77 The GT-4 patients are currently the most difficult to treat. New treatments are needed for unsuccessfully treated non-GT-1 patients: currently, the only option is a second course of PR, which results in poor SVR rates (19% to 34% for nonresponders and 46% for relapsers).78

Telaprevir and boceprevir in non-GT-1 patients

Telaprevir monotherapy has an antiviral activity against HCV GT-2, but not against GT-3.79 Triple therapy with telaprevir for 2 weeks for GT-2 patients leads to a greater drop of HCV RNA level compared to the SOC treatment.79 In a Phase IIa study with 24 GT-4 patients, triple therapy with telaprevir for 2 weeks induces a greater reduction of HCV RNA level compared to the SOC treatment. However, after the continuation of PR for 46 weeks, the SVR rates do not increase compared to the SOC treatment.80 The data on treatment with boceprevir is limited. Boceprevir monotherapy for 2 weeks induces a significant viral drop for GT-3 patients.81 However, no Phase II study exists for this population. Triple regimens with first-generation PIs have at most limited antiviral effectiveness in GT-3 and GT-4 patients; this confirms the need for more potent combinations with pan- or plurigenotypic activity.

Beyond first-generation PIs

The second-wave and second-generation PIs seem to have a better activity against multiple genotypes. Second-wave PIs have no activity against GT-3 but a good efficacy on GT-4 patients. Second-generation PIs (MK-5172, ACH-2684, AVL-181, AVL-192) are effective against all HCV genotypes in vitro.82

NIs (mericitabine and sofosbuvir) have similar efficacy against all genotypes and the highest barrier of resistance. Therefore, they appear to be among the most promising pan-genotypic drugs.35 On the other hand, NNIs demonstrate no antiviral activity against non-GT-1 patients.

NS5A.I also have an antiviral efficacy against all genotypes.46 The first-in-class NS5A.I demonstrate potent antiviral efficacy in triple regimen and in IFN-free regimen against GT-2, GT-3, and GT-4.

HTAs such as alisporivir demonstrate antiviral activities against GT-2, GT-3, and GT-4.83

Future GT-2 treatment

Simeprevir (TMC-435) monotherapy for 7 days demonstrates weak antiviral activity against GT-2 patients.84 MK-5172 appears to be more promising in this setting. A combination study with PR for 12 or 24 weeks is ongoing. After 4 weeks of triple regimen with mericitabine and PR for GT-2/3 treatment-failure patients, the RVR rate is 95% in the mericitabine arm versus 60% in the PR arm. Due to the short duration of the triple regimen, the high RVR rate does not transfer to a high SVR rate (only 63%).34 Sofosbuvir (GS-7977) 400 mg QD in association with PR for 12 weeks induces in Phase II studies an SVR for all patients. The same SVR rate is reached when naïve patients are treated in an IFN-free regimen with sofosbuvir and RBV for 12 weeks.35 For treatment-experienced patients, the same regimen for 12 weeks leads to an SVR rate of 68%. In Phase III studies (POSITRON and FISSION), IFN-free regimen with sofosbuvir and RBV for 12 weeks yields an SVR rate of 92%–97% for GT-2 naïve patients. For this population, IFN-free regimen with a combination of an NS5A.I and an NI appears to be of interest. A Phase II study combining daclatasvir and sofosbuvir with or without RBV for 24 weeks conducted with 44 GT-2 and GT-3 naïve patients demonstrates a 100% SVR rate among patients treated with DAAs only. The study shows that RBV, if added to this combination, does not increase the SVR rate.51 HTAs such as alisporivir may also play an important role in combination with DAAs. In a Phase II study (VITAL), 346 GT-2 and GT-3 naïve patients are randomized in 5 groups with different doses of ALV only or in combination with RBV with or without PEG-INF. In the three IFN-free arms, 22%, 23%, and 34% of the patients reach RVR and are therefore maintained on the IFN-free regimen until week 24. Twelve weeks after cessation of treatment, the SVR rates range from 82% to 93%.

This data suggests that the majority of GT-2 patients may soon be cured with a short course of DAA combination with or without RBV.

Future GT-3 treatment

Second-wave PIs have no effects on GT-3 patients. MK-5172 appears to be more promising; a combination study with PR for 12 or 24 weeks is ongoing. For GT-2 and GT-3 treatment-failure patients, 4 weeks of triple regimen with mericitabine and PR achieves an RVR rate of 95% (versus 60% for the PR arm). Again, the high RVR rate does not transfer to a high SVR rate (only 63%) due to the short duration of the triple regimen (see Future GT-2 treatment).34 In Phase II studies, sofosbuvir (GS-7977) 400 mg QD in association with PR for 12 weeks induces SVR for all patients. The same SVR rate is reached when naïve patients are treated in an IFN-free regimen with sofosbuvir and RBV for 12 weeks (see Future GT-2 treatment).35 SVR rates drop to 60% if sofosbuvir is used alone or if the RBV dose is reduced to 600 mg daily. As outlined in Section IIIc, the same regimen for 12 weeks leads to an SVR rate of 68% for treatment-experienced patients. In Phase III studies (POSITRON and FISSION), IFN-free regimen with sofosbuvir and RBV for 12 weeks results in an SVR rate of 56%–61% for GT-3 naïve patients. These results suggest that GT-3 patients are more difficult to cure with such short IFN-free regimens; a longer duration of treatment and association with other DAAs (like pan-genotypic NS5A.I) is needed. A Phase II study combining daclatasvir and sofosbuvir with or without RBV for 24 weeks conducted with 44 GT-2 and GT-3 naïve patients demonstrates a 100% SVR rate among patients treated with DAAs only. The study shows that RBV, if added to this combination, does not increase the SVR rate.51 HTAs such as alisporivir may also play an important role in combination with DAAs. In a Phase II study (VITAL), 346 GT-2 and GT-3 naïve patients are randomized in five groups with different doses of ALV only or in combination with RBV with or without PEG-INF. In the three IFN-free arms, 22%, 23%, and 34% of the patients reach RVR and are therefore maintained on the IFN-free regimen until week 24. Twelve weeks after cessation of treatment, the SVR rates range from 82% to 93% (see Future GT-2 treatment).

As for GT-2 patients, this data suggests that the majority of GT-3 patients may soon be cured with a short course of DAA combination with or without RBV. However, for some patients, combination therapy with PEG-INF and RBV is still required.

Future GT-4 treatment

Simeprevir monotherapy is able to induce a mean viral decrease of 3.52 log₁₀ IU/mL after 8 days of treatment for naïve GT-4 patients.84 Ritonavir-boosted danoprevir in association with PR for 24 weeks has cured all 29 GT-4 naïve patients treated so far.28 Asunaprevir is currently studied in an ongoing trial in combination with PR for various durations (24 to 48 weeks) for naïve GT-4 patients. Mericitabine in combination with PR appears to achieve comparable SVR rates to the SOC treatment for GT-4 naïve patients.85 Sofosbuvir 400 g daily in combination with PR for 24 weeks induces an end-of-treatment induces a SVR-rate of 82% in all eleven GT-4 naïve patients.39 Daclatasvir 60 mg daily in association with PR for 24 weeks reaches SVR for all 12 GT-4 naïve patients.47 There are two ongoing studies with GT-4 treatment-experienced patients. The first one evaluates the combination of daclatasvir, asunaprevir, and PR for 24 weeks; the second one evaluates the combination of ritonavir-boosted danoprevir, mericitabine and PR for 24 weeks. Moreover, there are several ongoing studies with IFN-free regimens for GT-4 naïve patients: the combination of ABT-450/r (PI), ABT-267 (NS5A.I), and RBV for 12 weeks; the combination of asunaprevir, daclatasvir plus BMS-790052 (NNI) for 12 or 24 weeks; the combination of sofosbuvir, ledipasvir (NS5A.I), and RBV for 12 weeks.

In conclusion, clinical results with DAAs are sparse for GT-4 patients. However, the reported results are promising, and suggest that the vast majority of GT-4 patients can be cured either with triple or quadruple regimen including PR. Also, IFN-free DAA combinations including PIs, NS5A.I, and NIs may be a good option.

Future GT-5 and GT-6 treatment

Clinical results concerning the use of DAAs for GT-5 and GT-6 HCV infections are limited.

Simeprevir monotherapy induces a significant mean decrease of viremia of 4.35 log₁₀ IU/mL after 8 days for the GT-6 patients; the mean decrease for GT-5 patients is only 2.19 log₁₀ IU/mL (2.71 log₁₀ IU/mL at day 3).84

Five GT-6 patients are included in the ATOMIC study. Under a combination therapy with sofosbuvir (GS-7977) 400 mg QD, PEG-INF, and RBV for 24 weeks, both the RVR rate at week 4 and the SVR rate 12 weeks after the end of the treatment are 100%.86

Cirrhotic patients

Cirrhotic patients require HCV treatment most urgently: HCV-clearance allows both a significant decrease of fibrosis and potential cirrhosis reversal and a significant decrease of cirrhosis-related complications.

Triple therapy with first-generation PIs

GT-1 patients with severe fibrosis or compensated cirrhosis benefit from adequate triple therapy with first-generation PIs, even if the increase of the SVR rate is less significant than for noncirrhotic patients.2–6

Compared to PR, a triple therapy with boceprevir leads to an increase of the SVR rate of 14% for naïve GT-1 cirrhotic patients. For patients with mild or moderate fibrosis, the SVR rate increases even by 30%.2 With telaprevir, the SVR rate increases by 10%–30% for cirrhotic patients, compared to 30% for noncirrhotic patients.3,4 Treatment-experienced patients benefit more from triple therapy with either boceprevir or telaprevir if they are previous relapsers than if they are partial responders.5,6 For null responders, the benefit is limited, and needs to be weighted against the increase of side effects.

Cirrhosis is one of the negative predictive factors for the response to triple therapy. In Phase III studies with boceprevir and telaprevir, cirrhotic patients have lower RVR rates, more frequent relapses, and always require long fixed duration therapy (4 weeks of PR lead-in followed by 44 weeks of triple regimen with boceprevir; 12 weeks of triple regimen with telaprevir followed by 36 weeks of PR).

In Phase III studies, serious adverse events occur for approximately 10% of the patients with both drugs. Serious adverse events are higher for cirrhotic patients. (Note however, that the number of cirrhotic patients in these studies is limited.) In the real-life setting of the French CUPIC cohort, which includes more than 600 treatment-experienced cirrhotic patients, it is demonstrated that the number of serious adverse events increases dramatically for cirrhotic patients after 16 weeks of treatments: by 38% with boceprevir and by 49% with telaprevir.87 Six patients died, mainly related to infection or hepatic decompensation. In multivariate analysis, two baseline factors are predictive for death infection or hepatic decompensation: platelet count <100,000/mm³ and serum albumin level <35 g/L. As expected, anemia is frequent and severe for cirrhotic patients treated with PIs in the CUPIC cohort. Despite the use of erythropoietin for nearly half of the patients, blood transfusion rate is high (6.3% with boceprevir and 16% with telaprevir after 16 weeks of treatment). This can partly be explained by the relatively small number of patients for whom the RBV dose was reduced (10% with boceprevir and 13% with telaprevir). The ITT analysis of preliminary virological results at week 16 shows that 67% of the patients treated with telaprevir and 58% of patients treated with boceprevir have undetectable HCV RNA. These good results need to be balanced with safety issues. Overall, triple therapy is feasible for cirrhotic patients who need to be carefully and frequently monitored during treatment.

Little data is available concerning the use of triple regimens in the post-transplant setting.88 The virological response during treatment appears to be promising. However, treatment is difficult due to very frequent hematological side effects. Drug–drug interactions with calcineurin inhibitors appear to be manageable by sizeable dose reduction of the calcineurin inhibitors.

Beyond first-generation PIs

Few data are available concerning second-wave PIs or other DAAs for cirrhotic patients.89 In a Phase IIb study, 83 GT-1 treatment-experienced cirrhotic patients are treated with simeprevir 100 or 150 mg QD and PR for 12, 24, or 48 weeks, followed by PR alone up to week 48. The SVR rates are 73% for previous relapsers, 82% for partial responders, and 31% for null responders (for those treated with 150 mg QD); in all cases, the SVR rates are higher than in the PR arms.16

For 23 GT-1/4 naïve cirrhotic patients treated with mericitabine 1000 mg BID and PR for 24 or 48 weeks, the SVR rate is 38% versus 22% in PR arms.32,33 However, dose or duration reduction of mericitabine impairs treatment response for cirrhotic patients. An ongoing study with GT-1 cirrhotic patients receiving quadruple regimen (mericitabine, ritonavir-boosted danoprevir, and PR) is currently being conducted.

Sofosbuvir was tested initially on 8 cirrhotic (CHILD-Pugh B) patients for 7 days (400 mg QD). The systemic exposure was the same for cirrhotic as for noncirrhotic patients, and a significant HCV RNA decline was observed. The decline for cirrhotic patients was less impressive than in patients with mild or moderate fibrosis.90 In the Phase III NEUTRINO study, sofosbuvir (400 mg QD) and PR for 12 weeks reaches an 80% SVR rate for 56 GT-1 cirrhotic patients.

Daclatasvir 20 or 60 mg QD in association with PR for 24 weeks reaches a SVR rate between 57% to 62% in 20 GT-1 naïve cirrhotic patients.47

INF-free regimen

Very few INF-free regimen studies include patients with cirrhosis. In SOUND-C2, one of the largest IFN-free regimen studies, 33 naïve GT-1 cirrhotic patients are treated with faldaprevir and BI-207127 with or without RBV for 16, 28, or 48 weeks. The SVR rates are 43%–50% for GT-1a patients and 57%–80% for GT-1b patients.91 These rates are close to those observed for the noncirrhotic population. Two Phase III studies investigate regimens with sofosbuvir 400 mg QD and RBV for 12 weeks with GT-2 or GT-3 patients. In the POSITRON study, the SVR rate is 61% among the 31 GT-2/3 cirrhotic patients; in the FISSION study, it is 47% (100 GT-2/3 cirrhotic patients).

Conclusion

Triple therapy with first-generation PIs was a major step forward in HCV treatment for GT-1 patients. Since 2010, more than ten different DAAs are in Phase II or III development. Approximately ten more DAAs are either in preclinical or in early clinical development. Meanwhile, several studies demonstrate that IFN-free regimens are able to cure a large number of either naïve or treatment-experienced GT-1 patients. Moreover, for the most difficult-to-cure patients, quadruple regimen with PR is able to cure almost all GT-1 null responders. The development of pan-genotypic DAAs such as NIs or NS5A.I allows new DAA combinations with or without PR; these increase the SVR rates for all patients (even for those with cirrhosis and for all genotypes). This new regimen appears so far to be safer, and also allows shorter treatment duration. These developments appear to be another major step forward for HCV treatment. Table 5 gives an estimated period on the timing that we could expect for the molecule to be launched. In conclusion, there is hope that almost all treated patients can be cured in the near future.

Table 5.

Estimate of first approval for the new HCV treatments in the USA and Europe

Protease inhibitor	Company	Current clinical phase	FDA approval expected	EMEA approval expected
Simeprevir TMC-43514,15	Tibotec	III	2013	2014
Faldaprevir BI-201 13516,17	Boehringer Ingelheim	III	2014	2014
Danoprevir (ITMN-191, RG 7227)18,19	Roche	II	2015?	2015 ?
Vaniprevir (MK-7009)20,21	Merck	III	No 2014(Japon)	No
ABT-45022	Abbott	III	2014	2014
Sovaprevir ACH-162523	Achillion	II	?	?
Asunaprevir BMS-65003224,25	BMS	III	2014	2014
GS-925667	Gilead	II	?	?
MK-5172	MSD	II	2015/2016	2015/2016
Polymerase inhibitors
RG-7128 Mericitabine 31–33	Roche	II	?	?
GS- 7977 Sofosbuvir34–38	Gilead	III	2013	2013
NNI-Site 1 inhibitors BI 207 12739	Bohringer Ingelheim	III	2014	2014
NNI-Site 1 inhibitors BMS 79132573	BMS	II	2014/2015	2014/2015
NNI-Site 2 inhibitors Filibuvir40	Pfizer	II	?	?
NNI-Site 2 inhibitors VX-22241	Vertex	II	?	?
NNI-Site 3 inhibitors Setrobuvir ANA59842	Anadys	I	?	?
NNI-Site 3 inhibitors ABT-33343	Abbott	III	2014	2014
NNI-Site 3 inhibitors ABT-07243	Abbott	II	?	?
NNI-Site 4 inhibitors Tegobuvir (GS9190)44	Gilead	II	?	?
NS5A-inhibitor
Daclatasvir (DCV) BMS-79005246–48	BMS	III	2014	2014
ABT 26751	Abbott	III	2014	2014
Ledipasvir GS-5885 www.clinicaltrial.gov	Gilead	III	2014	2014

Abbreviations: EMEA, European Medicines Agency; FDA, US Food and Drug Administration; HCV, hepatitis C virus.