Organization (Industry)
Concert Pharmaceuticals (United States)
ClinicalTrials.gov lists Concert Pharmaceuticals (United States) as lead sponsor of 33 trials. It has 3 active development programs and 8 approved assets.
Search trials, drugs, companies and investigators, and follow each one to the others. Individual plan, $249/seat/mo. Card required.
Trials started per year with this organization as sponsor or collaborator, 1990 onward. The series also counts trials where the organization is a collaborator; the lead-sponsor trial count does not.
2026 is partial: 0 registered with a 2026 start date. The dashed outline is the pace from the 0 registered with a start date through September, planned starts included, not adjusted; not a forecast. No forecast is made for this organization: it averages 1.2 trial starts a year over the five years to September, under the 5 a year the method needs.
This page covers Concert Pharmaceuticals (United States): 33 lead-sponsored trials and 1 legal-entity registration.
Disease areas (9)
Shown in this order: most trials first.
| Disease area | Trials |
|---|---|
| Alopecia | 6 |
| Alopecia Areata | 6 |
| Diabetes Mellitus | 2 |
| Renal Insufficiency, Chronic | 2 |
| Diabetes Mellitus, Type 2 | 1 |
Showing 5 of 9 disease areas.
Trials by start year as sponsor or collaborator (12)
Shown in this order: most recent first. 2026 is partial: trials registered with a 2026 start date so far, not a full year.
Show the table of trials by start year as sponsor or collaborator
| Year | Trials started |
|---|---|
| 2022 | 6 |
| 2021 | 4 |
| 2020 | 2 |
| 2019 | 7 |
| 2018 | 1 |
| 2017 | 1 |
| 2016 | 3 |
| 2015 | 3 |
| 2014 | 2 |
| 2012 | 1 |
Showing 10 of 12 years.
Recruitment duration, a model prediction: none of the 33 trials evaluated at the 2026-10-09 snapshot is predicted and still running. Source: ClinicalTrials.gov / AACT (CTTI), public domain.
Active development programs (3)
Shown in this order: max phase, then active trials.
| Drug | Disease area | Max phase | Trials |
|---|---|---|---|
| CTP-543 | Alopecia | Phase 3 | 6 |
| CTP-543 | Alopecia Areata | Phase 3 | 6 |
| CTP-692 | Schizophrenia | Phase 2 | 1 |
Approved assets (8)
Shown in this order: max phase first.
| Drug | Trials |
|---|---|
| CTP-543 | 17 |
| Ivacaftor | 2 |
| VX-561 | 2 |
| Fluconazole | 1 |
| MIDAZOLAM | 1 |
Showing 5 of 8 approved assets.
Sponsor delivery record (1)
Enrollment hit target: the share of this sponsor's lead-sponsored trials whose actual enrollment reached the planned enrollment. On time: the share whose actual primary completion date was no later than the planned date. Each share counts only trials where we observed an estimated figure before the actual one, and n is that number of trials. Below 5 trials the count is shown as a fraction, not a percentage.
| Enrollment | Timeline |
|---|---|
| 80% hit target (n=15) | 73% on time (n=15) |
Journals published in (1)
| Journal | Publications |
|---|---|
| Journal of the American Academy of Dermatology | 2 |
US granted patents (1)
Patents are not classified by disease area in the source, so this is the organization's overall portfolio, not a split by disease.
| US patents granted | Granted in the last 5 years | Most recent grant |
|---|---|---|
| 138 | 4 | 2025-06-03 |
Latest dated events (171)
Shown in this order: newest first.
| Date | Event | Source |
|---|---|---|
| 2025-06-03 | Patent granted | Granted US patents (PatentsView / USPTO) |
| 2022-10-18 | Patent granted | Granted US patents (PatentsView / USPTO) |
| 2022-07-11 | Trial started | Clinical trials (ClinicalTrials.gov) (ClinicalTrials.gov, U.S. National Library of Medicine; AACT database, Clinical Trials Transformation Initiative (CTTI)) |
| 2022-06-21 | Trial started | Clinical trials (ClinicalTrials.gov) (ClinicalTrials.gov, U.S. National Library of Medicine; AACT database, Clinical Trials Transformation Initiative (CTTI)) |
| 2022-06-14 | Trial started | Clinical trials (ClinicalTrials.gov) (ClinicalTrials.gov, U.S. National Library of Medicine; AACT database, Clinical Trials Transformation Initiative (CTTI)) |
Showing 5 of 171 events.
Biomarker capability evidence (4)
Shown in this order: tier desc, then gene symbol.
| Gene | Role | Evidence |
|---|---|---|
| CYP3A4 | Trial sponsor | Named in trial inclusion criteria |
| GGT1 | Trial sponsor | Named in trial exclusion criteria |
| CYP3A4 | Trial sponsor | Mentioned in trial text |
| GGT1 | Trial sponsor | Mentioned in trial text |
On Scientist.com
Concert Pharmaceuticals (United States) is listed as a research supplier in the Scientist.com network.
Service areas
We are a clinical stage biopharmaceutical company applying its extensive knowledge of deuterium chemistry to discover and develop novel small molecule drugs. Our approach starts with approved drugs, advanced clinical candidates or previously studied compounds that we believe can be improved with deuterium substitution to provide better pharmacokinetic or metabolic properties and thereby enhance clinical safety, tolerability or efficacy. We have executed on this approach to become a clinical stage biotechnology company and are developing a robust pipeline of product candidates in several...
Show the full description
We are a clinical stage biopharmaceutical company applying its extensive knowledge of deuterium chemistry to discover and develop novel small molecule drugs. Our approach starts with approved drugs, advanced clinical candidates or previously studied compounds that we believe can be improved with deuterium substitution to provide better pharmacokinetic or metabolic properties and thereby enhance clinical safety, tolerability or efficacy. We have executed on this approach to become a clinical stage biotechnology company and are developing a robust pipeline of product candidates in several therapeutic areas.
We apply our DCE Platform to systematically identify approved drugs, advanced clinical candidates or
previously studied compounds that we believe can be improved with deuterium substitution. Potential
advantages of our selective deuteration include:
Improved metabolic profile. We have selectively deuterated compounds or their metabolites to
improve their metabolic profiles. In some cases we also have reduced the formation of toxic or reactive
metabolites relative to the corresponding non-deuterated compound, thereby potentially eliminating
unwanted side effects or undesirable drug interactions.
Improved oral bioavailability. We have selectively deuterated compounds to reduce the extent of
undesired metabolism in the wall of the intestines and in the liver, referred to as first-pass metabolism.
This resulted in a larger percentage of unmetabolized drug reaching the target site of action.
Deuterated compounds with improved bioavailability may be active at lower doses.
Increased half-life. We have selectively deuterated compounds to increase their half-life in the body.
This may decrease the number of doses that a patient is required to take per day or provide more
consistent exposure of the compound in comparison to the corresponding non-deuterated compound.
- Website
- www.concertpharma.com
Not on this page
Checked, with nothing recorded for this organization: companies grouped under this page, related companies not grouped here, sec-reported annual financials, financing and grant events, fda warning letters, fda untitled letters, fda inspection record, fda recalls, fda import refusals, manufacturing and distribution sites, climate targets, as filed, workforce and board diversity, as filed, organization relationships, clia clinical laboratory certificates, and biomarkers this organization publishes on.
Work with Concert Pharmaceuticals on Scientist.com
For prices, more details, or to contact Concert Pharmaceuticals, visit Scientist.com.
Sign in to Scientist.com to open this supplier in your organization's marketplace.