TABLE 1.
Clinical trials of renin‐angiotensin system‐based therapies (including therapies targeting SARS‐Cov‐2 ACE2 interactions) listed in clinicaltrials.gov as of April 6, 2020
NCT number type of trial | Trial title | Listing date | Description (excerpted from listing) |
---|---|---|---|
NCT04287686 withdrawn as of 3/17/20 Viral decoy soluble ACE2 |
Recombinant Human Angiotensin‐converting Enzyme 2 (rhACE2) as a Treatment for Patients With COVID‐19 | 2/27/20 | An open label, randomized, controlled, pilot clinical study in patients with COVID‐19, to obtain preliminary biologic, physiologic, and clinical data in patients with COVID‐19 treated with rhACE2 or control patients, to help determine whether a subsequent phase 2B trial is warranted. |
Viral decoy circulating ACE2 with virus immuno‐neutralizing capability |
A phase I/II study of universal off‐the‐shelf NKG2D‐ACE2 CAR‐NK cells for therapy of COVID‐19 | 3/27/20 | This construct is a universal off‐the‐shelf IL15 superagonist‐ and GM‐CSF neutralizing scFv‐secreting NKG2D‐CAR‐NK expressing ACE2 on its cell surface to attract SARS‐CoV‐2. NKG2D is an activating receptor of NK cells, which can recognize and thus clear unbound SARS‐CoV‐2 virus particles as well as SARS‐CoV‐2 infected cells. |
Viral decoy soluble ACE2 |
Phase II clinical trial of APN01 (recombinant human ACE2 to treat COVID‐19) | 4/6/20 | Randomized double blind study of patients with severe COVID‐19 infections, to determine the efficacy of rhACE2 administration. |
Angiotensin II AT1 receptor blockade (ARB) to reduce COVID 19 pathology |
Losartan for patients with COVID‐19 requiring hospitalization | 3/17/20 | This is a multicenter, double‐blinded study of COVID‐19 infected patients requiring inpatient hospital admission randomized 1:1 to daily losartan or placebo for 7 days or hospital discharge. |
Angiotensin II AT1 receptor blockade (ARB) to reduce COVID 19 pathology |
Losartan for patients with COVID‐19 not requiring hospitalization | 3/17/20 | This is a multicenter, double‐blinded study of COVID‐19 infected patients randomized 1:1 to daily losartan or placebo for 10 days or treatment failure (hospital admission). |
Angiotensin II AT1 receptor blockade (ARB) to reduce COVID 19 morbidity |
Comparison of therapeutics for hospitalized patients infected with SARS‐CoV‐2 in a pragmatic aDaptive randoMizED Clinical Trial During the COVID‐19 Pandemic (COVID MED Trial) | 3/31/20 | Hospitalized patients: Group 1 standard care and lopinavir/ritonavir, Group 2 standard care and hydroxychloroquine, Group 3 standard care and losartan, or Group 4 standard care and placebo, will be followed for up to 60 days, with data collected to quantify the NIAID COVID‐19 ordinal severity scale (NCOSS) over time (the primary objective). Secondary objectives (a) length of hospital stay, (b) level of ICU care, (c) length of use of mechanical ventilation, (d) survival. |
Angiotensin II AT1 receptor blockade (ARB) to reduce lung pathology |
Valsartan for prevention of acute respiratory distress syndrome in hospitalized patients with SARS‐COV‐2 infection disease | 4/6/20 | Currently available AT1R blockers (ARBs) such as valsartan, have the potential to block pathological increases in pulmonary vascular permeability mediated by angiotensin (Ang) II through its Ang II Type 1 receptor (AT1R), when activity of ACE2 to metabolize ang II is decreased by SARS‐Cov‐2. |
Assess safety of angiotensin II AT1 receptor blockade (ARB) |
Study of open label losartan in COVID‐19 | 4/6/20 | Open label, phase 1 clinical trial to evaluate the safety of losartan in respiratory failure due to COVID‐19 |
Proactive study of Ang 1–7 to treat severe SARS‐CoV‐2 infections |
Angiotensin‐(1,7) treatment in COVID‐19: the ATCO Trial | 4/3/20 | To test the safety, efficacy and clinical impact of the infusion of angiotensin‐(1–7), the product of ACE2, in COVID‐19 patients with respiratory failure requiring mechanical ventilation. |
Discontinuation of angiotensin II AT1 receptor blockade (ARB) therapy |
ACE inhibitors or ARBs discontinuation in context of SARS‐CoV‐2 pandemia | 4/1/20 | Compare continuation of RAS blocker therapy with discontinuation of RAS blocker therapy |
Discontinuation or continuation of angiotensin II AT1 receptor blockade (ARB) therapy in COVID 19 patients |
Coronavirus ACEi/ARB Investigation | 4/1/20 | Continue ACEi/ARB antihypertensive or switch to an alternative BP medication (specifically a calcium channel blocker [CCB] or thiazide/thiazide‐like diuretic at an equipotent blood pressure lowering dose). |
Retrospective study of ACE inhibitor or ARB use to assess benefits or harms in SARS‐CoV‐2 infections |
Hypertension in patients hospitalized with COVID‐19 | 3/23/20 | There is a large number of patients with SARS‐CoV‐2 that have hypertension, suggesting that patients with hypertension may be more susceptible to covid19. This retrospective study will follow‐up patients admitted to Hankou hospital to explore the impact of hypertension and hypertension treatment on severity and prognosis of patients with SARS‐CoV‐2, |
Retrospective study of ACE inhibitor and ARB use to assess benefits or harms in SARS‐CoV‐2 infections |
ACE inhibitors, angiotensin II Type‐I receptor blockers and severity of COVID‐19 | 3/24/20 | To retrospectively test whether 2019‐nCoV patients treated with ACE‐I or ARB, compared with patients who not treated with ACE‐I or ARB, are at higher risk of having severe COVID‐19 (including death). |
Retrospective study of ACE inhibitor use relationship to the incidence of influenza |
The use of angiotensin‐converting enzyme inhibitors and incident respiratory infections, are they harmful or protective? | 3/26/20 | The study use UK based linked electronic health records from the clinical research datalink (CALIBER) of 5.6 million individuals to conduct a matched case–control study to investigate the incidence of influenza in individuals prescribed ACEI compared to those not prescribed ACEI. |
Retrospective study of antihypertensive medications and COVID 19 infection outcomes |
Comparison of therapeutics for hospitalized patients infected with SARS‐CoV‐2 in a Pragmatic aDaptive randoMizED Clinical Trial During the COVID‐19 Pandemic (COVID MED Trial) | 3/31/20 |
Assessment of cardiovascular diseases and cardiovascular risk factors At inclusion, patients will be screened for preexisting cardiovascular diseases and cardiovascular risk factors, as well as medication. |
Retrospective study of ARB and ACE inhibitor use relationship to the incidence of COVID‐19 infection |
Renin‐angiotensin system inhibitors and COVID‐19 | 4/2/20 | Using anamnestic data collected from the health record of the hospital or of the general practitioner, we will count the number of COVID‐19 patients enrolled that were treated with ACE inhibitors or ARBs to observe whether antihypertensive ACE inhibitors or ARBs increases the severity of the clinical manifestation of COVID19. |
Note: As of April 6, 2020 there are 16 trials listed with Clinicaltrials.gov: Three viral decoy studies, one of which has been withdrawn, five ARB therapy studies, one Ang 1–7 (product of ACE2) study, two withdrawal of ACE inhibitor or ARB therapy with or without antihypertensive drug replacement studies, and five retrospective studies of ARB or ACE inhibitor use relationship to COVID infection incidence and morbidity. Different types of studies are separated by shading differences.