Phase I Clinical Study of SHR-5495 in the Treatment of Patients With Advanced Malignant Tumors
Recruiting in Palo Alto (17 mi)
Age: 18+
Sex: Any
Travel: May Be Covered
Time Reimbursement: Varies
Trial Phase: Phase 1
Recruiting
Sponsor: Suzhou Suncadia Biopharmaceuticals Co., Ltd.
No Placebo Group
Trial Summary
What is the purpose of this trial?
This study is an open, multicenter, dose-increasing/dose-expanding/efficacy expanding Phase I clinical study aimed at evaluating the tolerance, safety, PK, PD, and immunogenicity of SHR-5495 in the treatment of advanced malignant tumor patients, and preliminarily observing its anti-tumor efficacy. The entire study was divided into three stages: dose escalation, dose extension, and efficacy extension.
Research Team
Eligibility Criteria
Inclusion Criteria
Your ECOG score must be between 0 and 1.
You are between 18 and 70 years of age, gender notwithstanding.
You have a pathologically confirmed advanced malignant tumor that has not responded to conventional treatment approaches or lacks an efficient standard treatment option.
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Treatment Details
Participant Groups
1Treatment groups
Experimental Treatment
Group I: SHR-5495 for injectionExperimental Treatment1 Intervention
Find a Clinic Near You
Who Is Running the Clinical Trial?
Suzhou Suncadia Biopharmaceuticals Co., Ltd.
Lead Sponsor
Trials
65
Recruited
15,600+
Dr. Tian Guanghui
Suzhou Suncadia Biopharmaceuticals Co., Ltd.
Chief Executive Officer since 2020
PhD in Chemical Engineering
Dr. Shen
Suzhou Suncadia Biopharmaceuticals Co., Ltd.
Chief Medical Officer since 2013
MD