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Compound · clinical trials

Velinotamig specified on specified days clinical trials

Also listed in trial records as CLN-803, GR1803
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 5 trials in our China and USA registers that name Velinotamig specified on specified days as an intervention. Synced 26 Sep 2026
5Current trials
2Recruiting now
2Lead sponsors
2Country registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 โ€” Top 14 finalist
Compiled from ClinicalTrials.gov registry records ยท Last verified ยท Editorial standards
At a glance

Velinotamig specified on specified days is named as an intervention in 5 current clinical trials in our China and USA registers. 2 are recruiting patients now. The most common phase is Phase 1/2. The sponsor with the most trials is Genrix (Shanghai) Biopharmaceutical Co., Ltd (4). The most-studied condition is Multiple Myeloma.

Trials by status

  • Recruiting240%
  • Not yet open240%
  • Active, closed120%

Trials by phase

  • Phase 1/2360%
  • Phase 3120%
  • Phase 2120%
01

Clinical trials of Velinotamig specified on specified days

5 trials
StudyPhaseStatusLead sponsorRegisters
A Study of GR1803 Injection Versus Daratumumab, Pomalidomide, and Dexamethasone (DPd) in Participants With Relapsed or Refractory Multiple Myeloma
NCT07452198 · ClinicalTrials.gov ↗ · Multiple Myeloma
Phase 3 Recruiting Genrix (Shanghai) Biopharmaceutical Co., Ltd. China
A Study of GR1803 in Systemic Lupus Erythematosus
NCT07348055 · ClinicalTrials.gov ↗ · Systemic Lupus Erthematosus, Auto Immune Disease
Phase 1/2 Recruiting Genrix (Shanghai) Biopharmaceutical Co., Ltd. China
A Study of GR1803 Injection in Combination With Anti-CD38 Monoclonal Antibody for the Treatment of Participants With Multiple Myeloma
NCT07090954 · ClinicalTrials.gov ↗ · Multiple Myeloma
Phase 1/2 Not yet open Genrix (Shanghai) Biopharmaceutical Co., Ltd. China
A Phase 1b/2a Study of Velinotamig in Adults With Relapsed/Refractory ITP and wAIHA
NCT07738822 · ClinicalTrials.gov ↗ · Immune Thrombocytopenia (ITP), Warm Autoimmune Hemolytic Anemia (WAIHA)
Phase 1/2 Not yet open Cullinan Therapeutics Inc. USA
GR1803 Injection in Patients With Relapsed/Refractory Multiple Myeloma
NCT06566547 · ClinicalTrials.gov ↗ · Multiple Myeloma
Phase 2 Active, closed Genrix (Shanghai) Biopharmaceutical Co., Ltd. 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. Trial titles and statuses are copied from the registry as published.

02

Conditions studied with Velinotamig specified on specified days

5 conditions
Multiple Myeloma3Immune Thrombocytopenia (ITP)1Warm Autoimmune Hemolytic Anemia (WAIHA)1Systemic Lupus Erthematosus1Auto Immune Disease1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Genrix (Shanghai) Biopharmaceutical Co., Ltd.4
Cullinan Therapeutics Inc.1
04

By country register

RegisterTrialsRecruiting
Clinical trials in China42
Clinical trials in USA10

A trial with sites in more than one country appears in each of those registers.

05

Related compounds

06

Questions about Velinotamig specified on specified days trials

How many clinical trials are testing Velinotamig specified on specified days?

5 current trials in our China and USA registers name Velinotamig specified on specified days (also registered as CLN-803) as a drug or biological intervention, as of the registry sync on 26 September 2026. Completed and withdrawn studies are not counted.

Are Velinotamig specified on specified days trials recruiting patients?

Yes. 2 of the 5 trials are recruiting: 2 with sites in China. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Velinotamig specified on specified days clinical trials?

Genrix (Shanghai) Biopharmaceutical Co., Ltd (4) and Cullinan Therapeutics Inc (1). 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 Velinotamig specified on specified days works or whether it is effective, and it is not medical advice.

How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records โ€” it is not written from memory, and nothing here describes how Velinotamig specified on specified days 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 Velinotamig specified on specified days (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 26 Sep 2026.

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 โ€” 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 โ€” we correct promptly and log it.