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Bioengineering & Translational Medicine logoLink to Bioengineering & Translational Medicine
. 2021 Aug 13;6(3):e10246. doi: 10.1002/btm2.10246

Nanoparticles in the clinic: An update post COVID‐19 vaccines

Aaron C Anselmo 1,, Samir Mitragotri 2,3,
PMCID: PMC8420572  PMID: 34514159

Abstract

Nanoparticles are used in the clinic to treat cancer, resolve mineral deficiencies, image tissues, and facilitate vaccination. As a modular technology, nanoparticles combine diagnostic agents or therapeutics (e.g., elements, small molecules, biologics), synthetic materials (e.g., polymers), and biological molecules (e.g., antibodies, peptides, lipids). Leveraging these parameters, nanoparticles can be designed and tuned to navigate biological microenvironments, negotiate biological barriers, and deliver therapeutics or diagnostic agents to specific cells and tissues in the body. Recently, with the Emergency Use Authorization of the COVID‐19 lipid nanoparticle vaccines, the advantages and potential of nanoparticles as a delivery vehicle have been displayed at the forefront of biotechnology. Here, we provide a 5‐year status update on our original “Nanoparticles in the Clinic” review (also a 2‐year update on our second “Nanoparticles in the Clinic” review) by discussing recent nanoparticle delivery system approvals, highlighting new clinical trials, and providing an update on the previously highlighted clinical trials.

Keywords: clinic, clinical translation, clinical trials, drug delivery, nanomedicine, nanoparticles, translational medicine

1. INTRODUCTION

Over the past 2 years, the nanomedicine landscape has evolved rapidly, driven by the worldwide clinical introduction of the Moderna and Pfizer‐BioNTech COVID‐19 lipid nanoparticle mRNA vaccines.1 Given this sudden expansion of nanoparticle use in the clinic, we are updating our “Nanoparticles in the Clinic” review and providing an update on the clinical landscape of nanomedicines. Our original review was published in 2016 and highlighted >25 approved nanomedicines and >45 unapproved nanoparticles that were being evaluated clinical trials.2 In 2019, our second review included three new nanoparticle approvals, added >75 new clinicals trials for the previously highlighted unapproved nanoparticles, and added >15 new nanoparticles that entered clinical trials.3 In this 2021 update, we provide a broad overview of the current clinical landscape by adding two nanoparticles that recently received Emergency Use Authorization (both in 2020), >30 new trials that have started for previously tabulated unapproved nanoparticles, and >35 new nanoparticle technologies (associated with >55 new trials) that have recently entered clinical trials.

2. UPDATES ON CURRENTLY APPROVED NANOPARTICLES AND NEW ADDITIONS

Over the past 2 years, the nanomedicine landscape has evolved rapidly, driven by the global need for new technologies to provide prophylactic and therapeutic approaches against the coronavirus disease 2019 (COVID‐19),4, 5, 6 which is caused by the severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2).7 Of the technologies that have emerged to combat COVID‐19, lipid nanoparticles are the delivery vehicle used in the Moderna and Pfizer‐BioNTech COVID‐19 vaccines, both of which were granted Emergency Use Authorization in the United States in 2020.8

The Moderna vaccine, mRNA‐1273, is a lipid nanoparticle consisting of the ionizable cationic lipid SM‐102 (heptadecan‐9‐yl 8 ((2 hydroxyethyl) (6 oxo 6‐(undecyloxy) hexyl) amino) octanoate), DSPC (1,2‐distearoyl‐snglycero‐3 phosphocholine), cholesterol, and PEG‐DMG (1 monomethoxypolyethyleneglycol‐2,3‐dimyristylglycerol with polyethylene glycol).9 mRNA‐1273 was granted Emergency Use Authorization by the U.S. FDA on December 18th, 2020,10 based on a number of clinical trials, including one that demonstrated anti‐SARS‐CoV‐2 immune responses in participants without trial‐limiting safety concerns11 and another clinical trial with 30,420 participants that demonstrated 94.1% efficacy at preventing COVID‐19 illness.12 The Pfizer‐BioNTech vaccine, BNT162b2, is also a lipid nanoparticle and consists of the ionizable cationic lipid ALC‐0315 ((4‐hydroxybutyl)azanediyl)bis(hexane‐6,1‐diyl)bis(2‐hexyldecanoate), DSPC (1,2‐distearoyl‐sn‐glycero‐3‐phosphocholine), cholesterol, and PEG‐DMA (2 [(polyethylene glycol)‐2000]‐N,N‐ditetradecylacetamide).9 BNT162b2 was granted Emergency Use Authorization by the U.S. FDA on December 11th, 2020,10 based on a number of clinical trials, including one that demonstrated both safety and immunogenicity of BNT162b2,13 and another clinical trial with 43,548 participants that demonstrated BNT162b2 was 95% effective in preventing COVID‐19.14 Both lipid nanoparticle formulations are administered intramuscularly in two separate doses and are used to encapsulate mRNA that encodes for the SARS‐CoV‐2 spike glycoprotein, which mediates attachment to host cells and thus enables viral entry.11 By encoding for this spike glycoprotein, the host generates an immune response to the presented antigenic proteins; thus, a neutralizing antibody response against SARS‐CoV‐2 is generated.15 In both formulations, lipid nanoparticles enable delivery of the sensitive mRNA cargo into the cytoplasm,16 which has been the major obstacle in translation of mRNA technologies.17 By overcoming the challenges of intracellular delivery using lipid nanoparticles, antigen presentation could occur and the neutralizing antibody response against SARS‐CoV‐2 was achieved. Collectively, mRNA‐1273 and BNT162b2 are used in >35 countries10 with an estimated 3 billion (2 billion for BNT162b2 and 1 billion for mRNA‐1273) doses to be manufactured throughout 2021.18

Table 1 has been updated to list FDA/EMA approved injectable nanomedicines up to 2021, including the lipid nanoparticle mRNA vaccines against COVID‐19. Figures 1 and 2 highlight key aspects of these tabulated findings. Figure 1 shows the chronological approvals of nanoparticles based on particle type. Lipid‐based and inorganic nanoparticles comprise the majority of clinically‐approved nanoparticles. Interestingly, the first (1989) and most recent (2020) clinically approved/authorized particles highlight how lipid‐based nanoparticles, as a platform technology, enable controlled interactions between encapsulated therapeutics and complex microenvironments within patients. While the majority of lipid‐based nanoparticles are approved and clinically‐used for intravenous applications, lipid‐based nanoparticles are also used to protect sensitive cargos (e.g., mRNA) after manufacturing, during storage, and during intramuscular muscular injection and throughout their action within the host. Figure 2 shows the chronological approvals of nanoparticles based on indication, with the dominant applications being cancer, anemia, and imaging.

TABLE 1.

Clinically approved nanoparticle therapies and diagnostics, grouped by their broad indication

Name Particle type Payload Approved application/indication Approval (year)
New additions
mRNA‐1273 (Moderna) Lipid nanoparticle mRNA COVID‐19 vaccine FDA, Emergency Use Authorization (2020)
Tozinameran/BNT162b2 (Pfizer‐BioNTech) Lipid nanoparticle mRNA COVID‐19 vaccine FDA, Emergency Use Authorization (2020)
Cancer

Doxil

Caelyx (Janssen)

PEGylated liposome Doxorubicin Ovarian cancer, HIV‐associated Kaposi's sarcoma, Multiple myeloma

FDA (1995)

EMA (1996)

DaunoXome (Galen) Liposome (non‐PEGylated) Daunorubicin HIV‐associated Kaposi's sarcoma FDA (1996)
Myocet (Teva UK) Liposome (non‐PEGylated) Doxorubicin Breast cancer

EMA (2000)

Abraxane (Celgene) Albumin‐particle Paclitaxel Advanced non‐small cell lung cancer, Metastatic pancreatic cancer, Metastatic breast cancer

FDA (2005)

EMA (2008)

Marqibo (Spectrum) Liposome (non‐PEGylated) Vincristine Philadelphia chromosome‐negative acute lymphoblastic leukemia FDA (2012)
MEPACT (Millennium) Liposome (non‐PEGylated) Mifamurtide Osteosarcoma EMA (2009)

NBTXR3

Hensify (Nanobiotix)

Hafnium oxide nanoparticles Stimulated with external radiation to enhance tumor cell death via electron production Squamous cell carcinoma CE Mark (2019)

Onivyde

MM‐398 (Merrimack)

PEGylated liposome Irinotecan Metastatic pancreatic cancer FDA (2015)

VYXEOS

CPX‐351 (Jazz Pharmaceuticals)

Liposome Cytarabine:daunorubicin (5:1 molar ratio) Acute myeloid leukemia

FDA (2017)

EMA (2018)

Iron‐replacement

CosmoFer

INFeD

Ferrisat (Pharmacosmos)

Iron dextran colloid Iron Iron deficient anemia

FDA (1992)

Some of Europe

DexFerrum

DexIron (American Regent)

Iron dextran colloid Iron Iron deficient anemia FDA (1996)
Ferrlecit (Sanofi) Iron gluconate colloid Iron Iron replacement for anemia treatment in patients with chronic kidney disease FDA (1999)
Venofer (American Regent) Iron sucrose colloid Iron Iron replacement for anemia treatment in patients with chronic kidney disease FDA (2000)

Feraheme (AMAG)

Rienso (Takeda)

Ferumoxytol

Iron polyglucose sorbitol carboxymethylether colloid Iron Iron deficiency in patients with chronic kidney disease FDA (2009)

Injectafer

Ferinject (Vifor)

Iron carboxymaltose colloid Iron Iron deficient anemia FDA (2013)
Monofer (Pharmacosmos) 10% iron isomaltoside 1000 colloid Iron Treating iron deficiency and anemia when oral methods do not work or when iron delivery is required immediately Some of Europe (2009)
Diafer (Pharmacosmos) 5% iron isomaltoside 1000 colloid Iron Iron deficient anemia

Some of Europe

(2013)

Imaging agents
Definity (Lantheus Medical Imaging) Lipid microspheres Perflutren Ultrasound contrast agent FDA (2001)

Feridex I.V. (AMAG)

Endorem

Iron dextran colloid Iron Imaging of liver lesions

FDA (1996)

Discontinued (2008)

Ferumoxtran‐10 Combidex

Sinerem (AMAG)

Iron dextran colloid Iron Imaging lymph node metastases Only available in the Netherlands (2013)
Optison (GE Healthcare) Human serum albumin stabilized microspheres Perflutren Ultrasound contrast agent

FDA (1997)

EMA (1998)

SonoVue (Bracco Imaging) Phospholipid stabilized microbubble Hexafluoride Ultrasound contrast agent EMA (2001)

Resovist (Bayer Schering Pharma)

Cliavist

Iron carboxydextran colloid Iron Imaging of liver lesions

Some of Europe (2001)

Discontinued (2009)

Vaccines
Epaxal (Crucell) Liposome Inactivated hepatitis A virus Hepatitis A vaccine Some of Europe (2003; Now discontinued)
Inflexal V (Crucell) Liposome Trivalent‐influenza virus surface antigens Influenza vaccine Some of Europe (1997; Now discontinued)
Anesthetics
Diprivan Liposome Propofol Induction and maintenance of sedation or anesthesia FDA (1989)
Amyloidosis

ONPATTRO

Patisiran

ALN‐TTR02 (Alnylam Pharmaceuticals)

Lipid nanoparticle RNAi for the knockdown of disease‐causing TTR protein Transthyretin (TTR)‐mediated amyloidosis

FDA (2018)

EMA (2018)

Fungal infections
AmBisome (Gilead Sciences) Liposome Amphotericin B

Cryptococcal Meningitis in HIV‐infected patients

Aspergillus, Candida and/or Cryptococcus species infections (secondary)

Visceral leishmaniasis parasite in immunocompromised patients

FDA (1997)

Most of Europe

Macular degradation
Visudyne (Bausch and Lomb) Liposomal Verteporfin Treatment of subfoveal choroidal neovascularization from age‐related macular degeneration, pathologic, or ocular histoplasmosis

FDA (2000)

EMA (2000)

Note: Recent nanoparticles that have received Emergency Use Authorization are separately listed in the first rows.

Source: Modified with permissions from References 2 and 3.

FIGURE 1.

FIGURE 1

Chronological nanoparticle approvals based on particle type

FIGURE 2.

FIGURE 2

Chronological nanoparticle approvals based on indication

In addition to this updated Table 1, we also report an update on the number of clinical trials for approved nanoparticles that have appeared since our previous two articles in 2016 and 20192, 3: Figure 3 shows the number of clinical trials for each of the approved nanoparticles (see Table S1 for detailed summary) from 2016 (red) to 2019 (blue) to 2021 (green). Of particular note, we observe: (i) an increase in the number of clinical trials for 21 of the 29 approved nanoparticles in Table 1 (excluding the newly‐added mRNA‐1723 and BNT162b2), and (ii) an increase in the total number of clinical trials for approved nanoparticles from 1220 (in 2016), to 1716 (in 2019), and to 1935 (in 2021). Together, this demonstrates the continued success of nanoparticles that are being introduced into the clinic and the continued investigation of already‐approved nanoparticles toward expanding or improving their clinical use.

FIGURE 3.

FIGURE 3

Chronological update on the number of clinical trials for each nanoparticle, based on the number of identified trials in our previous “Nanoparticles in the Clinic” reviews in 20162 and 2019.3 These trials and nanoparticles have appeared on the ClinicalTrial.gov databaseSource: Modified with permissions from References 2 and 3

3. UPDATE ON PREVIOUS CLINICAL TRIALS FOR UNAPPROVED NANOPARTICLES

In our previous article,3 >60 different non‐approved nanoparticles were listed as active in >100 clinical trials. Here, we are updating the current clinical landscape for each of these clinically investigated nanoparticles (Table 2). In this update, >40 new trials have been added. Regarding previous clinical trials that were available before 2019,3 11 have been updated to active status, 5 have been updated to recruiting status, 5 have been terminated, 8 have been updated to unknown status, 12 have been completed, 3 have been withdrawn, and 12 have posted results that are viewable on ClinicalTrials.gov (Table 2). Of particular note: (i) 10 new trials began for a mitoxantrone hydrochloride liposome, used for the treatment of various cancers, (ii) 11 new trials began for Sonazoid, which is a lipid‐encapsulated formulation of F‐butane for ultrasound imaging, and (iii) results have been posted for PNT2258, DCR‐MYC, SGT‐53, NK105, CRLX101, CRLX301, AuroLase, and Halaven. Table 2 provides a detailed tabulation of these recent updates.

TABLE 2.

Updates on previously reported nanoparticle clinical trials that are not clinically approved or authorized and are currently active in clinical trials

Name (company) Particle type Payload Investigated application/indication ClinicalTrials.gov identifiers (phase) Updates since 2019
Lipid‐based (cancer)

PROMITIL

(Lipomedix Pharmaceuticals)

PEGylated liposome Mitomycin‐C Solid tumors

2016:

NCT01705002 (Ph I): Completed

2019:

NCT03823989 (Ph Ib): Recruiting (Active as of 2021)

2021 additions:

NCT04729205 (Ph I): Recruiting

2021:

One new trial

One trial updated to active

2019:

One new trial

One trial updated to completed

ThermoDox®

(Celsion)

Lyso‐thermosensitive liposome Doxorubicin Various cancers

2016:

NCT02536183 (Ph I): Recruiting

NCT00826085 (Ph I/II): Completed

NCT02112656 (Ph III): Completed

NCT02181075 (Ph I): Completed

2019 additions:

NCT03749850 (Ph I): Not yet recruiting (Recruiting as of 2021)

2021 additions:

NCT04852367 (Ph I): Not yet recruiting

NCT04791228 (Ph II): Not yet recruiting

2021:

Two new trials

One trial updated to recruiting

2019:

One new trial

Three trials updated to completed

Oncoprex/GPX‐001

(Genprex)

Liposome FUS1 (TUSC2) Lung cancer

2016:

NCT01455389 (Ph I/II): Active, not recruiting

2021 additions:

NCT04486833 (Ph I/II): Not yet recruiting

2021:

One new trial

2019:

No updates

Halaven

E7389‐LF

(Eisai)

Liposome Eribulin mesylate Solid tumors

2016:

NCT01945710 (Ph I): Completed

2019 additions:

NCT03207672 (Ph I): Recruiting (Active as of 2021)

2021 additions:

NCT04078295 (Ph I/II): Recruiting

2021:

One new trial

One trial updated to recruiting

Results posted and viewable on ClinicalTrials.gov for NCT01945710

2019:

One new trial

One trial updated to completed

188Re‐BMEDA‐liposome Pegylated liposome 188Re‐N,N‐bis (2‐mercaptoethyl)‐N′,N′‐diethylethylenediamine Advanced solid tumors

2016:

NCT02271516 (Ph I): Unknown (Terminated as of 2021 due to concerns of accumulation of radioactivity in both the liver and spleen)

2021:

One trial updated to terminated

2019:

Zero new trials

Mitoxantrone Hydrochloride Liposome

(CSPC ZhongQi Pharmaceutical Technology)

Liposome Mitoxantrone Various cancers

2016:

NCT02131688 (Ph I): Unknown

NCT02596373 (Ph II): Recruiting (Unknown status as of 2021)

NCT02597387 (Ph II): Recruiting (Unknown status as of 2021)

NCT02595242 (Ph I): Withdrawn

NCT02597153 (Ph II): Terminated (Only one subject enrolled in 1.5 years)

2019 additions:

NCT03776279 (Ph I): Recruiting (Unknown status as of 2021)

2021 additions:

NCT04668690 (Ph III): Not yet recruiting

NCT04718402 (Ph I): Recruiting

NCT04902027 (Ph I): Not yet recruiting

NCT04719065 (Ph I): Recruiting

NCT04718376 (Ph I): Recruiting

NCT04900766 (Ph I): Not yet recruiting

NCT04548700 (Ph I): Not yet recruiting

NCT04509466 (Ph I): Not yet recruiting

NCT04331743 (Ph I): Not yet recruiting

NCT04352413 (Ph II): Recruiting

2021:

10 new trials

Three trials updated to unknown status

2019:

One new trial

One trial updated to withdrawn

One trial updated to terminated

JVRS‐100 Cationic liposome Plasmid DNA complex for immune system stimulation Leukemia

2016:

NCT00860522 (Ph I): Completed

2021:

No updates

2019:

Zero new trials

One trial updated to completed

Lipocurc

(SignPath Pharma)

Liposome Curcumin Solid tumors

2016:

NCT02138955 (Ph I/II): Unknown

2021:

No updates

2019:

Zero new trials

One trial updated to unknown status

LiPlaCis

(LiPlasome Pharma)

Liposome with specific degradation‐controlled drug release via phospholipase A2 (PLA2) Cisplatin Advanced or refractory tumors

2016:

NCT01861496 (Ph I): Recruiting (Active as of 2021)

2021:

One trial updated to active

2019:

No updates

MM‐302

(Merrimack Pharmaceuticals)

HER2‐targeted PEGylated liposome Doxorubicin Breast cancer

2016:

NCT01304797 (Ph I): Unknown

NCT02213744 (Ph II/III): Terminated (Felt not to show benefit over control per DMC and confirmed via futility analysis)

2019 additions:

NCT02735798 (Ph I): Withdrawn (The study was not started due to the sponsor choosing to not fund the trial)

2021:

No updates

2019:

One new trial (withdrawn)

One trial updated to terminated

One trial updated to unknown status

LIPUSU®

(Nanjing Luye Sike Pharmaceutical Co., Ltd.)

Liposome Paclitaxel Advanced solid tumors, or gastric, breast cancer

2016:

NCT01994031 (Ph IV): Unknown

NCT02142790 (Ph IV): Unknown

NCT02163291 (Ph II): Unknown

NCT02142010 (Not Provided): Unknown

2019 additions:

NCT02996214 (Ph IV): Not yet recruiting (Active as of 2021)

2021:

One trial updated to active

2019:

One new trial

TKM‐080301

(Arbutus Biopharma)

Lipid particle targeting polo‐like kinase 1 (PLK1) siRNA Hepatocellular carcinoma

2016:

NCT02191878 (Ph I/II): Completed

2021:

No updates

2019:

Zero new trials

One trial updated to completed

siRNA‐EphA2‐DOPC Liposome siRNA for EphA2 knockdown Solid tumors

2016:

NCT01591356 (Ph I): Recruiting (Active as of 2021)

2021:

One trial updated to active

2019:

Zero new trials

PNT2258

(ProNAi Therapeutics)

Lipid nanoparticle Proprietary single‐stranded DNAi (PNT100) Lymphomas

2016:

NCT02378038 (Ph II): Terminated

NCT02226965 (Ph II): Unknown (Completed as of 2021)

NCT01733238 (Ph II): Completed

2021:

Results posted and viewable on ClinicalTrials.gov for NCT02378038, NCT02226965, and NCT01733238

2019:

Zero new trials

One trial updated to completed

One trial updated to terminated

One trial updated to unknown status

BP1001/Prexigebersen

(Bio‐Path Holdings)

Neutral liposomes Growth factor receptor bound protein‐2 (Grb‐2) antisense oligonucleotide Leukemias and solid tumors

2016:

NCT01159028 (Ph I): Active, not recruiting (Updated to completed)

2019 additions:

NCT02923986 (Ph I): Recruiting (Withdrawn as of 2021 due to no enrollment)

NCT02781883 (Ph II): Recruiting

2021 additions:

NCT04196257 (Ph I): Not yet recruiting

2021:

One new trial

One trial updated to completed

One trial updated to withdrawn

2019:

Two new trials

DCR‐MYC

(Dicerna Pharmaceuticals)

Lipid nanoparticle DsiRNA for NYC oncogene silencing Solid tumors, multiple myeloma, lymphoma, or hepatocellular carcinoma

2016:

NCT02110563 (Ph I): Terminated (Sponsor Decision)

NCT02314052 (Ph I/II) Terminated (Sponsor Decision)

2021:

Results posted and viewable on ClinicalTrials.gov for NCT02314052

2019:

Zero new trials

Two trials updated to terminated

Atu027

(Silence Therapeutics GmbH)

Liposome AtuRNAi for PKN3 knockdown in vascular endothelium Pancreatic cancer

2016:

NCT01808638 (Ph I/II): Completed

2021:

No updates

2019:

Zero new trials

One trial completed

SGT‐53

(SynerGene Therapeutics)

Cationic liposome with anti‐transferrin receptor antibody Wildtype p53 sequence Glioblastoma, solid tumors, or pancreatic cancer

2016:

NCT02354547 (Ph I): Recruiting (Active as of 2021)

NCT02340156 (Ph II): Recruiting (Terminated as of 2021)

NCT00470613 (Ph I): Completed

2019 additions:

NCT03554707 (Ph I): Not yet recruiting

2021 additions:

NCT02340117 (Ph II): Recruiting

2021:

One new trial

Results posted and viewable on ClinicalTrials.gov for NCT02340156

2019:

One new trial

One trial updated to completed

SGT‐94

(SynerGene Therapeutics)

Liposome with anti‐transferrin receptor antibody RB94 plasmid DNA Solid tumors

2016:

NCT01517464 (Ph I): Completed

2021:

No updates

2019:

Zero new trials

One trial updated to completed

MRX34

(Mirna Therapeutics)

Liposome Double‐stranded RNA mimic of miR‐34

Liver cancer

2016:

NCT01829971 (Ph I): Terminated (Five immune related serious adverse events)

2019 additions:

NCT02862145 (Ph I): Withdrawn (five immune related serious adverse events in Phase 1 study)

2021:

No updates

2019:

One new trial (withdrawn)

One trial updated to terminated

TargomiRs

(EnGeneIC)

Anti‐EGFR bispecific antibody minicells (bacteria derived nanoparticles) miR‐16 based microRNA Mesothelioma and non‐small cell lung cancer

2016:

NCT02369198 (Ph I): Completed

2021:

No updates

2019:

Zero new trials

One trial updated to completed

MM‐310

(Merrimack Pharmaceuticals)

Liposome functionalized with antibodies targeted to the EphA2 receptor Docetaxel Solid tumors

2019:

NCT03076372 (Ph I): Recruiting (Unknown as of 2021)

2021:

No updates

EGFR(V)‐EDV‐Dox

(EnGeneIC)

Bacterially derived minicell Doxorubicin Recurrent glioblastoma

2019:

NCT02766699 (Ph I): Recruiting

2021:

No updates

Alprostadil liposome

(CSPC ZhongQi Pharmaceutical Technology)

Liposome

Alprostadil Safety and tolerability

2019:

NCT03669562 (Ph I): Recruiting (Unknown as of 2021)

2021 additions:

NCT04197323 (Ph II): Recruiting

2021:

One trial updated to active

One trial updated to unknown status

Liposomal Annamycin

(Moleculin Biotech)

Liposome Annamycin Acute myeloid leukemia

2019:

NCT03388749 (Ph II): Recruiting

NCT03315039 (Ph II): Recruiting (Active as of 2021)

2021 additions:

NCT04887298 (Ph I/II): Not yet recruiting

2021:

One new trial

One trial updated to active

FF‐10832

(Fujifilm Pharmaceuticals)

Liposome Gemcitabine Advanced solid tumors

2019:

NCT03440450 (Ph I): Recruiting

2021:

No updates

Anti‐EGFR‐IL‐dox

(Swiss Group for Clinical Cancer Research; University Hospital, Basel, Switzerland)

Anti‐EGFR immunoliposome Doxorubicin

Advanced triple negative EGFR positive breast cancer

High grade gliomas

2019:

NCT02833766 (Ph II): Recruiting (Active as of 2021)

NCT03603379 (Ph I): Recruiting (Completed as of 2021)

2021:

One trial updated to active

One trial updated to completed

TLD‐1/Talidox

(Swiss Group for Clinical Cancer Research)

Liposome Doxorubicin Advanced solid tumors

2019:

NCT03387917 (Ph I): Recruiting

2021:

No updates

NC‐6300

(NanoCarrier)

Micelle Epirubicin Advanced solid tumors or soft tissue sarcoma

2019:

NCT03168061 (Ph II): Recruiting

2021:

No updates

MRT5201

(Translate Bio)

PEGylated liposomes mRNA Ornithine transcarbamylase deficiency

2019:

NCT03767270 (Ph I): Not yet recruiting (Withdrawn as of 2021 due to program discontinuation)

2021:

One trial updated to withdrawn

Lipo‐MERIT

(BioNTech SE)

Liposome Four naked ribonucleic acid (RNA)‐drug products Cancer vaccine for advanced melanoma

2019:

NCT02410733 (Ph I): Recruiting (Active as of 2021)

2021:

One trial updated to active

BNT114/IVAC_W_bre1_uID

(BioNTech SE)

Patient‐specific liposome (specificity for antigen‐expression on a patient's tumor) Complexed RNA Triple negative breast cancer

2019:

NCT02316457 (Ph I): Recruiting (Active as of 2021)

2021:

One trial updated to active

Lipid‐based (other)

ND‐L02‐s0201

(Nitto Denko)

Lipid nanoparticle conjugated to Vitamin A siRNA

Hepatic fibrosis and pulmonary fibrosis

2016:

NCT02227459 (Ph I): Completed

2019 additions:

NCT01858935 (Ph I): Completed

NCT03241264 (Ph I): Completed

NCT03538301 (Ph II): Recruiting

2021:

No updates

2019:

Three new trials (two completed)

One trial updated to completed

ARB‐001467

TKM‐HBV

(Arbutus Biopharma)

Lipid particle Three RNAi therapeutics that target three sites on the HBV genome Hepatitis B

2016:

NCT02631096 (Ph II): Completed

2021:

No updates

2019:

Zero new trials

One trial updated to completed

CAL02

(Combioxin SA)

Cholesterol liposomes for toxin neutralization Sphingomyelin Pneumonia

2016:

NCT02583373 (Ph I): Completed

2021:

No updates

2019:

Zero new trials

One trial updated to completed

Nanocort/Sunpharma1505

(Enceladus in collaboration with Sun Pharma Global)

PEGylated liposome Prednisolone Rheumatoid arthritis and hemodialysis fistula maturation

2016:

NCT02495662 (Ph II): Terminated (Slow inclusion)

NCT02534896 (Ph III): Terminated

2021:

No updates

2019:

Zero new trials

Two trials updated to terminated

RGI‐2001

(Regimmune)

Liposome α‐GalCer Mitigating graft versus host disease following stem cell transplant

2016:

NCT01379209 (Ph I/II): Unknown (Completed as of 2021)

2019 additions:

NCT04014790 (Ph II): Not yet recruiting (Recruiting as of 2021)

2021 additions:

NCT04473911 (Ph I): Recruiting

2021:

One new trial

One trial updated to completed

One trial updated to recruiting

2019:

One new trial

Sonazoid Lipid shell F‐butane Contrast enhanced ultrasound for imaging hepatocellular carcinoma, skeletal muscle perfusion, or for estimating portal hypertension

2016:

NCT00822991 (Not Provided): Recruiting (Unknown status as of 2021)

NCT02398266 (Ph II): Unknown

NCT02188901 (Not Provided): Completed

NCT02489045 (Ph IV): Recruiting (Completed as of 2021)

2021 additions:

In 2021, there are 28 total studies

2021:

28 trials total (11 active trials were added after 2019)

2019:

Zero new trials

One trial updated to unknown status

One trial completed

mRNA‐1944

(Moderna)

Moderna's proprietary lipid nanoparticle technology Two mRNAs that encode heavy and light chains of anti‐Chikungunya antibody Safety, tolerability, pharmacokinetics and pharmacodynamics toward the prevention of Chikungunya virus infection

2019:

NCT03829384 (Ph I): Recruiting (Active as of 2021)

2021:

One trial updated to active

Polymeric and micelles (cancer)

AZD2811

(AstraZeneca with BIND Therapeutics)

BIND therapeutics polymer particle accruing platform Aurora B kinase inhibitor Advanced solid tumors

2016:

NCT02579226 (Ph I): Recruiting (Completed as of 2021)

2019 additions:

NCT03366675 (Ph II): Terminated (Early detection of the purpose of the study)

NCT03217838 (Ph I): Recruiting (Completed as of 2021)

2021 additions:

NCT04525391 (Ph II): Recruiting

NCT04745689 (Ph II): Recruiting

2021:

Two new trials

Two trials updated to completed

2019:

Two new trials (one terminated)

BIND‐014

(BIND Therapeutics)

PSMA targeted (via ACUPA) PEG‐PLGA or PLA–PEG particle Docetaxel Prostate, metastatic, non‐small cell lung, cervical, head and neck, or KRAS positive lung cancers

2016:

NCT02479178 (Ph II): Terminated

NCT02283320 (Ph II): Completed

NCT01812746 (Ph II): Completed

NCT01792479 (Ph II): Completed

NCT01300533 (Ph I): Completed

2021:

No updates

2019:

Zero new trials

Four trials updated to completed

Cynviloq

IG‐001

(Sorrento)

Polymeric micelle Paclitaxel Breast cancer

2016:

NCT02064829 (Not Provided): Completed

2021:

No updates

2019:

Zero new trials

One trial updated to completed

Genexol‐PM

(Samyang Biopharmaceuticals)

Polymeric micelle Paclitaxel Head and neck or breast cancer

2016:

NCT01689194 (Ph II): Unknown (Completed as of 2021)

NCT02263495 (Ph II): Completed

NCT00912639 (Ph IV): Unknown

2019 additions:

NCT02739633 (Ph II): Recruiting (Unknown as of 2021)

NCT03008512 (Ph II): Recruiting (Terminated as of 2021, due to poor accrual)

2021:

One trial updated to unknown status

One trial updated to terminated

2019:

Two new trials

One trial updated to completed

One trial updated to unknown status

NC‐6004 Nanoplatin

(Nanocarrier)

Polyamino acid and PEG micellar nanoparticle Cisplatin Advanced solid tumors, lung, biliary, bladder, or pancreatic cancers

2016:

NCT02240238 (Ph I/II): Active, not recruiting (Completed as of 2021)

NCT02043288 (Ph III): Unknown (Completed as of 2021)

2019 additions:

NCT03771820 (Ph II): Not yet recruiting (Recruiting as of 2021)

NCT03109158 (Ph I): Completed

NCT02817113 (Ph I): Unknown (Terminated as of 2021 due to strategy change)

2021:

Two trials updated to completed

One trial updated to recruiting

One trial updated to terminated

2019:

Three new trials

One trial updated to unknown status

NC‐4016 DACH‐Platin micelle

(Nanocarrier)

Polyamino acid and PEG micellar nanoparticle Oxaliplatin Advanced solid tumors or lymphomas

2016:

NCT01999491 (Ph I): Completed

2021:

No updates

2019:

Zero new trials

NK105

(Nippon Kayaku)

Micelle Paclitaxel Breast cancer

2016:

NCT01644890 (Ph III): Completed

2021:

Results posted and viewable on ClinicalTrials.gov for NCT01644890

2019:

Zero new trials

One trial completed

Docetaxel‐PM

DOPNP201

(Samyang Biopharmaceuticals)

Micelle Docetaxel Head and neck cancer and advanced solid tumors

2016:

NCT02639858 (Ph II): Recruiting (Unknown as of 2021)

NCT02274610 (Ph I): Completed

2019 additions:

NCT03585673 (Ph II): Recruiting (Unknown as of 2021)

2021 additions:

NCT04066335: Recruiting

2021:

One new trial

Two trials updated to unknown

2019:

One new trial

One trial updated to completed

CriPec

(Cristal Therapeutics)

Micelle Docetaxel Solid tumors, ovarian cancer

2016:

NCT02442531 (Ph I): Completed

2019 additions:

NCT03712423 (Ph I): Recruiting (Completed as of 2021)

NCT03742713 (Ph II): Recruiting (Completed as of 2021)

2021:

Two trials updated to completed

2019:

Two new trials

One trial updated to completed

CRLX101

(Cerulean)

Cyclodextrin based nanoparticle Camptothecin Ovarian, renal cell, small cell lung, or rectal cancers

2016:

NCT02187302 (Ph II): Completed

NCT02010567 (Ph I/II): Active, not recruiting (Terminated as of 2021 due to funding partner's request)

NCT02389985 (Ph I): Terminated (Company decision)

NCT01803269 (Ph II): Terminated (Due to lack of activity and slow accrual)

NCT01652079 (Ph II): Completed

2019 additions:

NCT02769962 (Ph I): Recruiting

NCT03531827 (Ph II): Recruiting

NCT02648711(Ph I): Terminated (Company decision)

NCT01380769 (Ph II): Completed NCT01612546 (Ph II): Completed

NCT00333502 (Ph II): Completed

NCT01625936 (Ph I): Completed

NCT00753740 (Ph II): Withdrawn (Poor trial recruitment)

NCT00163319 (Ph III): Completed

2021:

One trial updated to terminated

Results posted and viewable on ClinicalTrials.gov for NCT01380769, NCT01803269, and NCT02010567

2019:

Nine new trials (one terminated, one withdrawn, five completed)

Two trials updated to completed

Two trials updated to terminated

CRLX301

(Cerulean)

Cyclodextrin based nanoparticle Docetaxel Dose escalation study in advanced solid tumors

2016:

NCT02380677 (Ph I/II): Terminated (Company decision)

2021:

Results posted and viewable on ClinicalTrials.gov for NCT02380677

2019:

Zero new trials

One trial updated to terminated

MTL‐CEBPA

(Mina Alpha)

SMARTICLES (amphoteric liposomes) Double stranded RNA Advanced liver cancer and solid tumors

2019:

NCT02716012 (Ph I): Recruiting (Active as of 2021)

2021 additions:

NCT04105335 (Ph I): Recruiting

NCT04710641 (Ph II): Not yet recruiting

2021:

Two new trials

One trial updated to active

Imx‐110

(Immix Biopharma Australia)

Micelle Stat3/NF‐kB/poly‐tyrosine kinase inhibitor and low‐dose doxorubicin Advanced solid tumors

2019:

NCT03382340 (Ph I/II): Recruiting

2021:

No updates

IT‐141

(Intezyne Technologies)

Micelle SN‐38 Advanced cancer

2019:

NCT03096340 (Ph I): Recruiting (terminated as of 2021)

2021:

One trial updated to terminated

Polymeric and micelles (other)

RadProtect

(Original BioMedicals)

PEG, iron, and amifostine micelle

Transferrin‐mediated chelation for amifostine release

Amifostine Dose escalation and safety for acute radiation syndrome

2016:

NCT02587442 (Ph I): Unknown

2021:

No updates

2019:

Zero new trials

Albumin‐bound (cancer)

ABI‐009

(Aadi with Celgene)

Albumin‐bound drug nanoparticle Rapamycin Bladder cancer, PEComa, or pulmonary arterial hypertension

2016:

NCT02009332 (Ph I/II): Recruiting (Completed as of 2021)

NCT02587325 (Ph I): Recruiting

NCT02494570 (Ph II): Active not recruiting

2019 additions:

NCT03747328 (Ph II): Not yet recruiting

NCT03657420 (Ph I): Not yet recruiting (Withdrawn as of 2021)

NCT03670030 (Ph II): Recruiting (Completed as of 2021)

NCT03646240 (Ph I): Recruiting

NCT03190174 (Ph I): Recruiting

NCT00635284 (Ph I): Completed

NCT03817515: Expanded Access Status: Available

NCT03439462 (Ph II): Recruiting

NCT03463265 (Ph II): Recruiting

NCT03660930 (Ph I): Recruiting

NCT02975882 (Ph I): Recruiting

NCT02646319 (Ph I): Completed

2021:

Two trials updated to completed

2019:

12 new trials (two completed)

ABI‐011

(NantBioScience)

Albumin‐bound drug nanoparticle Thiocolchicine analog (IDN 5405) Solid tumors or lymphomas

2016:

NCT02582827 (Ph I): Recruiting (Withdrawn as of 2021 due to enrollment not initiated)

2021:

One trial updated to withdrawn

2019:

Zero new trials

Inorganic (cancer)

AuroLase

(Nanospectra Biosciences)

PEG‐coated silica‐gold nanoshells Thermal ablation from near infrared light stimulation Thermal ablation of solid primary and/or metastatic lung tumors

2016:

NCT01679470: Terminated

2019 additions:

NCT02680535: Recruiting (Completed as of 2021)

NCT00848042: Completed

2021 additions:

NCT04240639: Recruiting

2021:

One new trial

One trial updated to completed

Results posted and viewable on ClinicalTrials.gov for NCT00848042

2019:

Two new trials

One trial updated to terminated

Cornell Dots Silica nanoparticles with a NIR fluorophore, PEG coating, and a 124I radiolabeled cRGDY targeting peptide NIR fluorophore Imaging of melanoma and malignant brain tumors

2016:

NCT01266096: Active, not recruiting

2019 additions:

NCT03465618 (Ph I): Recruiting

NCT02106598 (Ph II): Recruiting

2021 additions:

NCT04167969 (Ph I): Recruiting

2021:

One new trial

2019:

Two new trials

Magnablate Iron nanoparticles Iron Thermal ablation for prostate cancer

2016:

NCT02033447 (Ph I): Completed

2021:

No updates

2019:

Zero new trials

One trial updated to completed

NU‐0129

(Northwestern)

Spherical nucleic acid platform consisting of nucleic acids arranged on the surface of a spherical gold nanoparticle Nucleic acids Glioblastoma

2019:

NCT03020017 (Ph I): Active, not recruiting (Completed as of 2021)

2021:

No updates

Imaging

AGuIX

(National Cancer Institute, France)

Polysiloxane gadolinium chelates based nanoparticles Gadolinium chelates Various cancers

2019:

NCT03308604 (Ph I): Recruiting (Unknown as of 2021)

2021 additions:

NCT04881032 (Ph I/II): Not yet recruiting

NCT03818386 (Ph II): Recruiting

NCT04899908 (Ph II): Not yet recruiting

NCT04094077 (Ph II): Active, not recruiting

NCT04789486 (Ph I/II): Not yet recruiting

NCT04784221 (Ph II): Not yet recruiting

2021:

Six new trials

One trial updated to unknown status

ONM‐100

(OncoNano Medicine)

Micelle covalently conjugated to indocyanine green Indocyanine green Intraoperative detection of cancer

2019:

NCT03735680 (Ph II): Not yet recruiting (Recruiting as of 2021)

2021:

One trial updated to recruiting

Note: These trials are grouped by particle type and indication.

Source: Modified with permissions from References 2 and 3.

4. NEW NANOPARTICLE TECHNOLOGIES IN CLINICAL TRIALS

Since our 2019 article,3 >35 new nanoparticle technologies have begun clinical trials. Of these new additions, 28 are lipid‐based (25 of which are for mRNA‐based vaccines). The remaining new nanoparticle technologies are indicated for cancer treatment (two pure‐drug nanoparticles are being studied in five different clinical trials), imaging applications (three trials are investigating carbon nanoparticles for imaging lymph nodes), and non‐mRNA vaccines (three protein‐based nanoparticles are being investigated as vaccines). Table 3 summarizes these new additions.

TABLE 3.

Nanoparticle vaccines, therapies, and diagnostics which are not clinically approved and are currently active clinical trials that have appeared on the ClinicalTrial.gov database since 2019

Name (company) Particle type Payload Investigated application/indication Current ClinicalTrials.gov identifiers (phase)
Lipid‐based

mRNA‐1283

(Moderna)

Lipid nanoparticle mRNA COVID‐19 vaccine NCT04813796 (Ph I): Recruiting

mRNA‐1345

(Moderna)

Lipid nanoparticle mRNA Respiratory syncytial virus vaccine NCT04528719 (Ph I): Recruiting

mRNA‐1647

(Moderna)

Lipid nanoparticle mRNA Cytomegalovirus vaccine NCT04232280 (Ph II): Recruiting

mRNA‐1653

(Moderna)

Lipid nanoparticle mRNA Combined human metapneumovirus and parainfluenza virus type 3 vaccine NCT04144348 (Ph I): Recruiting

mRNA‐2416

(Moderna)

Lipid nanoparticle mRNA Advanced solid tumor malignancies NCT03323398 (Ph I/II): Recruiting

mRNA‐2752

(Moderna)

Lipid nanoparticle mRNA Advanced solid tumor malignancies

NCT03739931 (Ph I): Recruiting

NCT02872025 (Ph I): Recruiting

mRNA‐4157

(Moderna)

Lipid nanoparticle mRNA Personalized cancer vaccine

NCT03313778 (Ph I): Recruiting

NCT03897881 (Ph II): Recruiting

mRNA‐5671/V941

(Merck)

Lipid nanoparticle mRNA KRAS vaccine NCT03948763 (Ph I): Recruiting

AZD8601

(AstraZeneca)

Lipid nanoparticle mRNA Personalized cancer vaccine

NCT03313778 (Ph I): Recruiting

NCT03897881 (Ph II): Recruiting

MEDI1191

(MedImmune)

Lipid nanoparticle mRNA Advanced solid tumors NCT03946800 (Ph I): Recruiting

DS‐5670a

(Daiichi Sankyo)

Lipid nanoparticle mRNA COVID‐19 Vaccine NCT04821674 (Ph I/II): Recruiting

BNT111

(BioNTech)

Size‐ and charge‐based RNA‐lipoplex nanoparticles for targeting dendritic cells RNA that elicits immune response against four antigens Metastatic melanoma vaccine NCT04526899 (Ph II): Recruiting

BNT112

(BioNTech)

Size‐ and charge‐based RNA‐lipoplex nanoparticles for targeting dendritic cells RNA that enables expression of five antigens Prostate cancer vaccine NCT04382898 (Ph I/II): Recruiting

BNT113

(BioNTech)

Size‐ and charge‐based RNA‐lipoplex nanoparticles for targeting dendritic cells RNA that elicits immune response against oncoproteins E6 and E7 Head and neck cancer vaccine NCT04534205 (Ph II): Recruiting

BNT115

(BioNTech)

mRNA‐lipoplex nanoparticles mRNA that increases tumor associated antigen expression Ovarian cancer NCT04163094 (Ph I): Recruiting

BNT122/RO7198457

(BioNTech and Genentech)

Size‐ and charge‐based RNA‐lipoplex nanoparticles for targeting dendritic cells RNA that encodes neoantigens Colorectal cancer, melanoma, lung cancer, bladder cancer

NCT04486378 (Ph II): Recruiting

NCT03815058 (Ph II): Recruiting

NCT03289962 (Ph I): Recruiting

BNT141

(BioNTech)

Liver‐targeting lipid nanoparticle mRNA that enables systemic production of IgG antibodies Solid tumors NCT04710043 (Ph I): Not yet recruiting

BNT151

(BioNTech)

Liver‐targeting lipid nanoparticle mRNA that enables systemic production of IL‐2 Solid tumors NCT04455620 (Ph I/II): Recruiting

BNT152 + BNT153

(BioNTech)

Liver‐targeting lipid nanoparticle mRNA that enables systemic production of IL‐7 and IL‐2 Multiple solid tumors NCT04710043 (Ph I): Not yet recruiting

CLDN6 RNA‐LPX

(BioNTech)

Size‐ and charge‐based RNA‐lipoplex nanoparticles for targeting dendritic cells RNA that encodes a receptor against CLDN6 Solid tumor NCT04503278 (Ph I/II): Recruiting

CVnCoV

(CureVac)

Lipid nanoparticle mRNA COVID‐19 vaccine

NCT04860258 (Ph III): Recruiting

NCT04838847 (Ph III): Recruiting

NCT04674189 (Ph III): Recruiting

NCT04652102 (Ph II/III): Active, not recruiting

NCT04515147 (Ph II): Active, not recruiting

NCT04449276 (Ph I): Active, not recruiting

NCT04848467 (Ph III): Not yet recruiting

CV7202

(CureVac)

Lipid nanoparticle mRNA encoding rabies virus glycoprotein Rabies vaccine NCT03713086 (Ph I): Active, not recruiting

ARCT‐021/LUNAR‐COV19

(Arcturus)

Lipid‐enabled and unlocked nucleomonomer agent mRNA (LUNAR®) mRNA COVID‐19 vaccine

NCT04728347 (Ph II): Recruiting NCT04668339 (Ph II): Active, not recruiting

NCT04480957 (Ph I/II): Recruiting

ARCT‐810/LUNAR‐OTC

(Arcturus)

Lipid‐enabled and unlocked nucleomonomer agent mRNA (LUNAR®) mRNA that enables synthesis of ornithine transcarbamylase enzyme Ornithine transcarbamylase deficiency NCT04442347 (Ph I): Recruiting

BP1002

(Bio‐Path Holdings)

Liposome Antisense designed to inhibit protein synthesis of Bcl‐2 Advanced lymphoid malignancies NCT04072458 (Ph I): Recruiting
SpFN_1B‐06‐PL + ALFQ (U.S. Army Medical Research and Development Command) Army liposomal formulation (adjuvant) Spike‐ferritin‐nanoparticle (vaccine) COVID‐19 Vaccine NCT04784767 (Ph I): Recruiting

HDT‐301

(SENAI CIMATEC)

Lipid‐Inorganic Nanoparticle (LION™); 15‐nm superparamagnetic iron oxide repRNA COVID‐19 Vaccine (repRNA) NCT04844268: (Ph I): Not yet recruiting

NTLA‐2001

(Intellia Therapeutics)

Lipid nanoparticles CRISPR/Cas9 for knockout edit to reduce transthyretin Transthyretin amyloidosis NCT04601051 (Ph I): Recruiting
Pure drug

NanoDoce®

(NanOlogy)

Large surface area microparticles (nanoparticulates) Docetaxel Urothelial carcinoma

NCT03636256 (Ph I/II): Active, not yet recruiting

NCT04060628: Available

NanoPac®

(NanOlogy)

Large surface area microparticles (nanoparticulates) Paclitaxel Pancreatic adenocarcinoma, lung cancer

NCT04314895 (Ph II): Recruiting

NCT03077685 (Ph II): Recruiting

NCT03756311: Available

Polymeric

PRECIOUS‐01

(Radboud University)

Poly(lactic‐co‐glycolic acid) (PLGA) nanoparticle Threitolceramide‐6 and the New York Esophageal Squamous Cell Carcinoma‐1 cancer‐testis antigen peptides New York Esophageal Squamous Cell Carcinoma‐1 positive cancers NCT04751786 (Ph I): Recruiting
Protein‐based

GBP510

(SK Bioscience Co.)

Self‐assembling protein nanoparticle immunogens Various immunogens COVID‐19 vaccine

NCT04742738 (Ph I/II): Recruiting

NCT04750343 (Ph I/II): Recruiting

NanoFlu

(Novavax)

Recombinant hemagglutinin protein nanoparticle with saponin‐based Matrix‐M adjuvant Recombinant hemagglutinin protein Influenza vaccine NCT04120194 (Ph III): Active, not recruiting

NVX‐CoV2373

SARS‐CoV‐2 rS/Matrix‐M1 adjuvant

(Novavax)

Recombinant spike protein nanoparticle with saponin‐based Matrix‐M1 adjuvant Recombinant spike protein COVID‐19 vaccine

NCT04611802 (Ph III): Recruiting

NCT04368988 (Ph I/II): Active, not recruiting

NCT04533399 (Ph II): Recruiting

NCT04583995 (Ph III): Recruiting

Inorganic

SPIONS

(Second Affiliated Hospital, School of Medicine, Zhejiang University)

Superparamagnetic iron oxide nanoparticles (SPIONs) with spinning magnetic field Superparamagnetic iron oxide nanoparticles Osteosarcoma NCT04316091 (Ph I): Not yet recruiting

EO2002

(Emmecell)

Magnetic nanoparticles with cultured human corneal endothelial cells Cultured human corneal endothelial cells Corneal edema NCT04894110 (Ph I): Recruiting

Carbon nanoparticles

(YE Yingjiang)

Carbon nanoparticles Carbon nanoparticle Lymph node tracer in rectal cancer NCT03550001: Not yet recruiting

Carbon nanoparticles

(The First Affiliated Hospital with Nanjing Medical University)

Carbon nanoparticles Carbon nanoparticle Lymph node tracer in breast cancer NCT04482803: Recruiting

Carbon nanoparticles

(LI XIN‐XIANG)

Carbon nanoparticles Carbon nanoparticle Lymph node tracer in colorectal cancer NCT04759820 (Ph II/III): Recruiting

Note: Trials are grouped by particle type.

5. CONCLUSION

The transformative role of lipid nanoparticles as mRNA delivery vehicles for combating COVID‐19 and their tremendous global impact during 2020 and 2021 has ushered in an unprecedented period for nanoparticle therapeutics. To date, >30 nanoparticles have been used in various clinical applications (Table 1) and >20 of these continue to be developed, with chronologically increasing activity in clinical trials (Figure 3 and Table S1). Of the 60 unapproved nanoparticle technologies currently being investigated in clinical trials, >100 active trials exist with >40 being added in this update alone (Table 2). Finally, since our previous update in 2019,3 there has been a massive surge in clinical introduction of new nanoparticle technologies, dominated by lipid nanoparticles for mRNA delivery; over 35 new nanoparticle technologies have entered clinical trials since 2019 (Table 3). Considering these recent updates and the global impact of nanoparticles in the clinic, especially as it relates to combating COVID‐19, the field of nanoparticle drug delivery is entering a new phase, wherein their development,19, 20 manufacturing,21, 22 and clinical utility23 is just beginning to scratch the surface.

AUTHOR CONTRIBUTIONS

Aaron Anselmo: Conceptualization; data curation; formal analysis; supervision; writing ‐ original draft; writing‐review & editing. Samir Mitragotri: Conceptualization; formal analysis; supervision; writing ‐ original draft; writing‐review & editing.

Supporting information

Appendix S1: Supporting information

ACKNOWLEDGMENTS

Samir Mitragotri acknowledges support from John A. Paulson School of Engineering & Applied Sciences and National Institutes of Health (1R01HL143806‐01).

Anselmo AC, Mitragotri S. Nanoparticles in the clinic: An update post COVID‐19 vaccines. Bioeng Transl Med. 2021;6(3):e10246. 10.1002/btm2.10246

Funding information National Heart, Lung, and Blood Institute, Grant/Award Number: 1R01HL143806‐01; John A. Paulson School of Engineering & Applied Sciences

Contributor Information

Aaron C. Anselmo, aanselmo@email.unc.edu.

Samir Mitragotri, Email: mitragotri@seas.harvard.edu.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Appendix S1: Supporting information


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