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Anti-CD20/CD3 Bispecific Antibody JS203 clinical trials

studies test it
3
open now
1
in phase 3
1
first study started
2023

How each study uses Anti-CD20/CD3 Bispecific Antibody JS203 is sorted by a rule, right about nine times in ten. Readers can ask us to read every study one by one.Ask us to read each study

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Approvals

The first approval found in each region, with its record

United States
Not in FDA's approval records
European Union
Not in EMA's list of EU-wide authorisations

From FDA's Drugs@FDA and Purple Book (through openFDA) and the European Medicines Agency, files of Sept 2026 and 27 Oct 2026. National approvals in Europe and other countries are not included. How this is worked out

How studies write it

Studies that test it under each name

In one entry with another drug

Given together, or one or the other

JS203 in combination with gemcitabine and oxaliplatin
2

Studies by the year they started

3 studies that test it; most in 2023 (1)

Studies that test Anti-CD20/CD3 Bispecific Antibody JS203, by start year
YearStudies
20231
20251
20261

By phase

A phase 1/2 study counts in both.

Phase 1
1
Phase 2
1
Phase 3
1

What it is tested for

Each study’s main condition, where its own words name it, so a study counts once.

Lymphoma, Large B-Cell, Diffuse
1

Who runs them

Industry 0 · Other 3

Shanghai Junshi Bioscience Co., Ltd. (3)

Coming up

From the study records. Dates are the sponsors’ own estimates and often move.

Reaching primary completion within a year · 2

Studies that test Anti-CD20/CD3 Bispecific Antibody JS203.

Studies

Open first, then newest update. How each study uses Anti-CD20/CD3 Bispecific Antibody JS203 is read from its arms, and is right about nine times in ten. Ask us to read each study. These are the studies that list it as an intervention; a search of ClinicalTrials.gov also finds studies that mention it only in a description, such as earlier treatment.

Testing it · 3