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Compound · clinical trials

SHR-9839

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 6 trials in our China register that name SHR-9839 as an intervention. Synced 24 Sep 2026
6Trials tracked
6Recruiting now
2Lead sponsors
1Country register
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

SHR-9839 is named as a drug or biological intervention in 6 clinical trials in our China trial register, 6 of which are recruiting. Lead sponsors include Suzhou Suncadia Biopharmaceuticals Co., Ltd. (4) and Shanghai Hengrui Pharmaceutical Co., Ltd. (2). Registered phases: Phase 1/2, Phase 1 and Phase 2. Conditions studied include Solid Tumor; Advanced Solid Tumors; Advanced Solid Tumor.

01

Clinical trials of SHR-9839

6 trials
NCT IDStudyPhaseStatusLead sponsorRegister
NCT07751341 A Clinical Study of SHR-9839 as Monotherapy or in Combination With Chemotherapy Plus Adebrelimab Versus Chemotherapy Plus Adebrelimab in Patients With Advanced Esophageal Squamous Cell Carcinoma (ClinicalTrials.gov ↗)
Advanced Esophageal Squamous Cell Carcinoma
Phase 2 Recruiting Suzhou Suncadia Biopharmaceuticals Co., Ltd. China
NCT06474455 A Phase IB/II Clinical Study of SHR-9839 for Injection Combined With Other Anti-tumor Therapies in Patients With Advanced Solid Tumors (ClinicalTrials.gov ↗)
Advanced Solid Tumors
Phase 1/2 Recruiting Shanghai Hengrui Pharmaceutical Co., Ltd. China
NCT06754930 A Study of SHR-1826 for Injection in Combination With Other Antitumor Therapies in Subjects With NSCLC (ClinicalTrials.gov ↗)
Non-small Cell Lung Cancer (NSCLC)
Phase 1/2 Recruiting Suzhou Suncadia Biopharmaceuticals Co., Ltd. China
NCT07059221 A Trial of SHR-A2102 With Adebrelimab With or Without Other Anti-tumor Therapies in Recurrent/MetastaticHead and Neck Squamous Cell Carcinoma Cancer (ClinicalTrials.gov ↗)
Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma
Phase 1/2 Recruiting Suzhou Suncadia Biopharmaceuticals Co., Ltd. China
NCT07229638 A IB/II Phase Clinical Study on the Safety, Tolerability, and Efficacy of SHR-9839(sc) in Combination Anti-tumor Therapy in Patients With Solid Tumors (ClinicalTrials.gov ↗)
Solid Tumor
Phase 1/2 Recruiting Suzhou Suncadia Biopharmaceuticals Co., Ltd. China
NCT05836948 The Clinical Study of SHR-9839 for Injection in Patients With Advanced Solid Tumors (ClinicalTrials.gov ↗)
Advanced Solid Tumor
Phase 1 Recruiting Shanghai Hengrui Pharmaceutical 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

6 conditions
Condition (as registered)Trials
Solid Tumor1
Advanced Solid Tumors1
Advanced Solid Tumor1
Advanced Esophageal Squamous Cell Carcinoma1
Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma1
Non-small Cell Lung Cancer (NSCLC)1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Suzhou Suncadia Biopharmaceuticals Co., Ltd.4
Shanghai Hengrui Pharmaceutical Co., Ltd.2
04

Trials by country register

RegisterSHR-9839 trials
Clinical trials in China6

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

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 SHR-9839 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 SHR-9839 (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 24 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.