Corvus Pharmaceuticals is the lead sponsor of 5 current clinical trials in our USA, China and EU (CTIS) registers. 3 are recruiting patients now. The most common phase is Phase 1. The drugs named most often in its trials are Soquelitinib and Pralatrexate. The most-studied condition is Peripheral T-Cell Lymphoma, Not Otherwise Specified.
| Study | Phase | Status | Start | Registers |
|---|---|---|---|---|
|
Soquelitinib vs Standard of Care in Participants With Relapsed/Refractory Peripheral T-cell Lymphoma Not Otherwise Specified, Follicular Helper T-cell Lymphomas, or Systemic Anaplastic Large-cell Lymphoma
NCT06561048 · Peripheral T-Cell Lymphoma, Not Otherwise Specified, Angioimmunoblastic T-cell Lymphoma, Follicular T-Cell Lymphoma
Drugs: Pralatrexate, Soquelitinib |
Phase 3 | Recruiting | 2024-10 | USA |
|
Study to Evaluate Soquelitinib in Participants With Moderate to Severe AD
NCT07441395 · ClinicalTrials.gov ↗ · Atopic Dermatitis, Atopic Dermatitis Eczema, Eczema
Drug: Soquelitinib |
Phase 2 | Recruiting | 2026-02 | USA |
|
Safety and Efficacy of Soquelitinib in Adults With Hidradenitis Suppurativa
NCT07828860 · ClinicalTrials.gov ↗ · Hidradenitis Suppurativa (HS)
Drug: Soquelitinib |
Phase 1 | Recruiting | 2026-09 | USA |
|
A Dose Escalation Study Evaluating CPI-818 in Relapsed/Refractory T-Cell Lymphoma
NCT03952078 · T-cell Lymphoma
|
Phase 1 | Active, closed | 2019-05 | USA, China |
Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Titles and statuses are copied from the registry as published.
Authorised or ongoing trials in the EU Clinical Trials Information System with Corvus Pharmaceuticals as sponsor. Some are the same study as a ClinicalTrials.gov record above; the two registries share no common ID. Trials with a site in Ireland are listed first.
| Study | Phase | Status | Countries |
|---|---|---|---|
|
A Phase 2 Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, and Preliminary Efficacy of Soquelitinib in Moderate to Severe Atopic Dermatitis (SIERRA1)
2025-524384-20-00 · Skin and Connective Tissue Diseases
Drug: Soquelitinib |
Phase 2 | Authorised | Italy, Czechia, Germany + 2 more |
Drugs and biologicals named as interventions in these trials, with the number of this sponsor's trials that name each one. Placebos and generic comparators are excluded.
| Register | Trials | Recruiting |
|---|---|---|
| Clinical trials in USA | 4 | 3 |
| Clinical trials in China | 1 | 0 |
| EU register (CTIS) | 1 | — |
A trial with sites in more than one country appears in each of those registers.
Corvus Pharmaceuticals is the lead sponsor of 4 current trials on ClinicalTrials.gov in our USA and China registers, and 1 authorised or ongoing trial in the EU register (CTIS), as of the registry sync on 26 September 2026. Completed and withdrawn studies are not counted.
Yes. 3 of its 4 ClinicalTrials.gov trials are recruiting. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.
Its current trials name 2 drugs and biologicals as interventions. The most frequent are Soquelitinib (4) and Pralatrexate (1). The number in brackets is how many of its trials name each drug.
Every trial, status, phase and condition on this page is copied from public ClinicalTrials.gov and EU CTIS records by a daily sync, grouped by the sponsor name each registry records. It says nothing about the organisation beyond its registered trials, and it is not medical advice.
Everything on this page is copied from public registry records — it is not written from memory, and nothing here describes the organisation beyond its registered trials. Each trial links to its own record so you can check it yourself.
This page is built automatically: a daily sync job reads the registry records behind our trial registers and groups every current trial by its lead sponsor name, ignoring legal-form suffixes such as Inc. or Ltd. A small, hand-checked list joins the same organisation's different registry names (for example its EU legal entity). There is no AI drafting and no per-sponsor editorial pass. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The the registries data on this page was last retrieved on 26 Sep 2026.