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Shanghai Escugen Biotechnology clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — current trials in our China register with Shanghai Escugen Biotechnology as lead sponsor. Synced 26 Sep 2026
4Current trials
2Recruiting now
1Drug in these trials
1Trial register
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 — Top 14 finalist
Compiled from ClinicalTrials.gov and CTIS registry records · Last verified · Editorial standards
At a glance

Shanghai Escugen Biotechnology is the lead sponsor of 4 current clinical trials in our China register. 2 are recruiting patients now. The most common phase is Phase 2. The drugs named most often in its trials are ESG206. The most-studied condition is Systemic Lupus Erythematosus (SLE).

ClinicalTrials.gov trials by status

  • Recruiting250%
  • Not yet open250%

Trials by phase

  • Phase 2250%
  • Phase 1125%
  • Phase 1/2125%
01

Clinical trials sponsored by Shanghai Escugen Biotechnology

4 on ClinicalTrials.gov
StudyPhaseStatusStartRegisters
Study of ESG406 in Adults With Solid Tumors
NCT06979674 · ClinicalTrials.gov ↗ · Locally Advanced/Metastatic Solid Tumors
Phase 1 Recruiting 2025-06 China
A Phase 1/2 Study of ESG206 in Patients With Primary Immune Thrombocytopenia
NCT06853444 · ClinicalTrials.gov ↗ · Immune Thrombocytopenia (ITP)
Drug: ESG206
Phase 1/2 Recruiting 2025-05 China
A Phase 2 Study on the Safety and Efficacy of the Anti-BAFF-R Monoclonal Antibody, ESG206, in Patients With Systemic Lupus Erythematosus
NCT07760155 · ClinicalTrials.gov ↗ · Systemic Lupus Erythematosus (SLE)
Drug: ESG206
Phase 2 Not yet open 2026-09 China
A Phase 2 Study on the Safety and Efficacy of the Anti-BAFF-R Monoclonal Antibody, ESG206, in Patients With Primary Sjogren Syndrome
NCT07375524 · ClinicalTrials.gov ↗ · Primary Sjögren Syndrome
Drug: ESG206
Phase 2 Not yet open 2026-03 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.

02

Drugs in Shanghai Escugen Biotechnology trials

1 compound

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.

03

Conditions in Shanghai Escugen Biotechnology trials

4 conditions
Systemic Lupus Erythematosus (SLE)1Primary Sjögren Syndrome1Locally Advanced/Metastatic Solid Tumors1Immune Thrombocytopenia (ITP)1
04

By trial register

RegisterTrialsRecruiting
Clinical trials in China42

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

05

Other sponsors in Systemic Lupus Erythematosus (SLE)

SponsorTrials
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology5
China Immunotech (Beijing) Biotechnology4
Beijing GoBroad Hospital3
EMD Serono Research & Development Institute2
Fate Therapeutics2
Bioray Laboratories2
iCell Gene Therapeutics1
Nanjing Legend Biotech Co1
Sunshine Guojian Pharmaceutical (Shanghai)1
Candid Therapeutics1

Sponsors with the most current trials registered for this condition.

06

Questions about Shanghai Escugen Biotechnology trials

How many clinical trials does Shanghai Escugen Biotechnology sponsor?

Shanghai Escugen Biotechnology is the lead sponsor of 4 current trials on ClinicalTrials.gov in our China register, as of the registry sync on 26 September 2026. Completed and withdrawn studies are not counted.

Are Shanghai Escugen Biotechnology trials recruiting?

Yes. 2 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.

Which drugs is Shanghai Escugen Biotechnology testing?

Its current trials name 1 drug or biological as interventions. The most frequent are ESG206 (3). The number in brackets is how many of its trials name each drug.

Where does this information come from?

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.

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How this page is built

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.

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.