Ireland
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Priya Life Science Compound trial record
Compound · clinical trials

Soquelitinib clinical trials

Also listed in trial records as CPI-818
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 4 trials in our USA, Australia, China, South Korea and Canada registers that name Soquelitinib as an intervention. Synced 10 Nov 2026
4Current trials
3Recruiting now
1Lead sponsor
5Country registers
At a glance

Soquelitinib is named as an intervention in 4 current clinical trials in our USA, Australia, China, South Korea and Canada registers. 3 are recruiting patients now. The most common phase is Phase 1. The lead sponsor is Corvus Pharmaceuticals, Inc. The most-studied condition is T-cell Lymphoma. The EU clinical trials register (CTIS) separately lists 1 authorised or ongoing trial.

Where Soquelitinib is approved

All regulators →
USUnited States (FDA)
No FDA approval of a single-substance product in Drugs@FDA
First original NDA/BLA approval
EUEuropean Union (EMA)
No centralised EU authorisation (it may be authorised nationally)
First centralised authorisation
CACanada (Health Canada)
No new-drug Notice of Compliance since 1994
First new-drug NOC

From the regulators' own registers: FDA Drugs@FDA, the EMA medicines list and Health Canada's Notice of Compliance database. Dates are the first listed approval of a product containing only this substance; combination products and nationally authorised EU medicines are not counted.

How Soquelitinib works

All drug targets →
Diseases it has been tested for in clinical trials, by furthest phase
  • Peripheral T-cell lymphoma, not otherwise specifiedPhase 3
  • Atopic eczemaPhase 2
  • Autoimmune lymphoproliferative syndromePhase 2
  • T-cell non-Hodgkin lymphomaPhase 1

Mechanisms and diseases from ChEMBL via the Open Targets Platform (release 26.09), ChEMBL record CHEMBL5817577, CC BY-SA 3.0. Targets checked against the IUPHAR/BPS Guide to PHARMACOLOGY (2026.3.1), ligand 13190, CC BY-SA 4.0. Trial phases are not approvals: approved uses are shown from the regulators' own records where we hold them.

Patient leaflets for Soquelitinib

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

  • UK
    United Kingdom: Search MHRA Products
    Patient information leaflets and SmPCs for UK-licensed products.
  • US
    United States: Search DailyMed
    FDA-approved labels, including patient and medication guides.

Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.

Trials by status

  • Recruiting375%
  • Active, closed125%

Trials by phase

  • Phase 1250%
  • Phase 3125%
  • Phase 2125%
01

Clinical trials of Soquelitinib

4 trials
StudyPhaseStatusLead sponsorRegisters
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
Phase 3 Recruiting Corvus Pharmaceuticals, Inc USA, Canada, Australia
Study to Evaluate Soquelitinib in Participants With Moderate to Severe AD
NCT07441395 · Atopic Dermatitis, Atopic Dermatitis Eczema, Eczema
Phase 2 Recruiting Corvus Pharmaceuticals, Inc USA
Safety and Efficacy of Soquelitinib in Adults With Hidradenitis Suppurativa
NCT07828860 · Hidradenitis Suppurativa (HS)
Phase 1 Recruiting Corvus Pharmaceuticals, Inc USA
A Dose Escalation Study Evaluating CPI-818 in Relapsed/Refractory T-Cell Lymphoma
NCT03952078 · T-cell Lymphoma
Phase 1 Active, closed Corvus Pharmaceuticals, Inc USA, China, South Korea, Australia

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. Trial titles and statuses are copied from the registry as published.

02

Soquelitinib in the EU trials register (CTIS)

1 trial

Authorised or ongoing trials in the EU Clinical Trials Information System that list a product containing Soquelitinib. Many trials are registered in both CTIS and ClinicalTrials.gov, so these are shown separately rather than added to the count above. Trials with a site in Ireland are listed first.

StudyPhaseStatusSponsorCountries
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
Phase 2 Ongoing Corvus Pharmaceuticals Inc Italy, Czechia, Germany + 3 more
03

Conditions studied with Soquelitinib

10 conditions
T-cell Lymphoma1Peripheral T-Cell Lymphoma, Not Otherwise Specified1Angioimmunoblastic T-cell Lymphoma1Follicular T-Cell Lymphoma1Nodal Peripheral T-Cell Lymphoma With TFH Phenotype1Atopic Dermatitis1Atopic Dermatitis Eczema1Eczema1Eczema, Atopic1Hidradenitis Suppurativa (HS)1
04

Sponsors

lead sponsor per trial
Lead sponsorTrials
Corvus Pharmaceuticals, Inc4
05

By country register

RegisterTrialsRecruiting
Clinical trials in USA43
Clinical trials in Australia21
Clinical trials in China10
Clinical trials in South Korea10
Clinical trials in Canada11
EU register (CTIS)1—

A trial with sites in more than one country appears in each of those registers. CTIS does not publish a recruiting flag; its trials may also appear in the registers above.

06

Related compounds

07

Questions about Soquelitinib trials

How many clinical trials are testing Soquelitinib?

4 current trials in our USA, Australia, China, South Korea and Canada registers name Soquelitinib (also registered as CPI-818) as a drug or biological intervention, as of the registry sync on 10 November 2026. Completed and withdrawn studies are not counted.

Are Soquelitinib trials recruiting patients?

Yes. 3 of the 4 trials are recruiting: 3 with sites in USA, 1 with sites in Australia and 1 with sites in Canada. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Soquelitinib clinical trials?

The lead sponsor is Corvus Pharmaceuticals, Inc. The number in brackets is how many trials each organisation leads.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how Soquelitinib works or whether it is effective, and it is not medical advice.

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How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how Soquelitinib works or whether it is effective. 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 country trial registers, collects every trial that lists Soquelitinib (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. 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 ClinicalTrials.gov data on this page was last retrieved on 10 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.