Ireland
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Priya Life Science Compound trial record
Compound · clinical trials

CD19 clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 2 trials in our China register that name CD19 as an intervention. Synced 9 Nov 2026
2Current trials
1Recruiting now
2Lead sponsors
1Country register
At a glance

CD19 is named as an intervention in 2 current clinical trials in our China register. 1 is recruiting patients now. The most common phase is Phase 1/2. The sponsor with the most trials is The First Affiliated Hospital of Soochow University (1). The most-studied condition is Acute Lymphoblastic Leukemia, Adult B-Cell.

Where CD19 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.

Patient leaflets for CD19

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

  • Recruiting150%
  • Active, closed150%

Trials by phase

  • Phase 1/2150%
  • Early Phase 1150%
01

Clinical trials of CD19

2 trials
StudyPhaseStatusLead sponsorRegisters
Clinical Study on Targeted CD19 or CD19-BCMA CAR-T Therapy for Autoimmune Diseases
NCT06548607 · ClinicalTrials.gov ↗ · SLE (Systemic Lupus), Systemic Sclerosis, ANCA Associated Vasculitis
Early Phase 1 Recruiting Nanjing Bioheng Biotech Co., Ltd China
CD19 CAR-T Consolidation Therapy for Acute Lymphoblastic Leukemia
NCT03984968 · ClinicalTrials.gov ↗ · Acute Lymphoblastic Leukemia, Adult B-Cell
Phase 1/2 Active, closed The First Affiliated Hospital of Soochow University 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 CD19

5 conditions
Acute Lymphoblastic Leukemia, Adult B-Cell1SLE (Systemic Lupus)1Systemic Sclerosis1ANCA Associated Vasculitis1Idiopathic Inflammatory Myopathies1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
The First Affiliated Hospital of Soochow University1
Nanjing Bioheng Biotech Co., Ltd1
04

By country register

RegisterTrialsRecruiting
Clinical trials in China21

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

05

Questions about CD19 trials

How many clinical trials are testing CD19?

2 current trials in our China register name CD19 as a drug or biological intervention, as of the registry sync on 9 November 2026. Completed and withdrawn studies are not counted.

Are CD19 trials recruiting patients?

Yes. 1 of the 2 trials is recruiting: 1 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 CD19 clinical trials?

The First Affiliated Hospital of Soochow University (1) and Nanjing Bioheng Biotech Co., Ltd (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 CD19 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 CD19 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 CD19 (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 9 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.