SHR-4375 for Solid Tumors

A Study of SHR-4375 in Subjects With Solid Tumors

Recruiting Phase 1 Phase 2 Interventional Study
Solid Tumors
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 1/2
Study type
Interventional
Purpose
Treatment
Participants needed
208 (estimated)
Sponsor
Suzhou Suncadia Biopharmaceuticals Co., Ltd. · Industry
Who this trial is looking for

This trial is looking for people with solid tumors who have not responded to standard treatments. Participants will receive an injection of SHR-4375 and help researchers learn about its safety and effectiveness.

Are You a Good Fit for This Trial?

You may be able to join if

  • I have signed the consent form to join this study.
  • I have a measurable disease.
  • I have an ECOG performance status of 0 or 1.
  • I expect to live for at least 12 weeks.
  • I have advanced solid tumors that have not responded to standard therapy, or I cannot take standard therapy, or I do not want standard therapy.

You may not be able to join if

  • I have untreated or active central nervous system metastases.
  • I have an active autoimmune disease or a history of autoimmune disease.
  • I have active hepatitis B or hepatitis C.
  • I have had severe infections before starting the study treatment.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

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About This Trial

This is an open-label, three-part study to evaluate the safety and efficacy of SHR-4375 for injection in subjects with solid tumors.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. The subjects voluntarily joined the study and signed the ICF. 2. Measurable disease, as defined by RECIST v1.1. 3. The Eastern Cancer Cooperative Group (ECOG) performance status of 0 or 1. 4. Life expectancy ≥ 12 weeks. 5. Subjects with cytologically or histologically confirm…
Contacts

Yuanchao Wang

0518-82342973

yuanchao.wang@hengrui.com

CONTACT