Phase I Clinical Study of SHR-5495 in the Treatment of Patients With Advanced Malignant Tumors
Study Details
Study Description
Brief Summary
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.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 1 |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: SHR-5495 for injection
|
Drug: SHR-5495 for injection
SHR-5495 for injection
|
Outcome Measures
Primary Outcome Measures
- Dose limited toxicity (DLT) of SHR-5495 [up to 21 days]
- AEs+SAEs [from the first drug administration to within 90 days for the last treatment dose]
- Maximum tolerated dose（MTD）of SHR-5495 [up to 21 days]
- Maximum administrated dose（MAD）of SHR-5495 [up to 21 days]
- Recommended Phase II Dose (RP2D) of SHR-5495 [up to 21 days]
Secondary Outcome Measures
- Evaluation of pharmacokinetic parameter of SHR-5495: Cmax [12 months]
- Evaluation of pharmacokinetic parameter of SHR-5495: Tmax [12 months]
- Evaluation of pharmacokinetic parameter of SHR-5495: AUClast [12 months]
- Evaluation of pharmacokinetic parameter of SHR-5495: AUCinf [12 months]
- Evaluation of pharmacokinetic parameter of SHR-5495: t1/2 [12 months]
- Evaluation of pharmacokinetic parameter of SHR-5495: CL [12 months]
- Evaluation of pharmacokinetic parameter of SHR-5495: Vss [12 months]
- Receptor occupancy rate [12 months]
- Objective Response Rate (ORR) [From date of administration until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 12 months]
- Duration of response (DoR) [From date of administration until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 12 months]
- Disease control rate (DCR) [From date of administration until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 12 months]
- Progression free survival（PFS） [From date of administration until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 12 months]
- Overall survival (OS) [From date of administration until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 12 months]
Eligibility Criteria
Criteria
Inclusion Criteria:
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Age range from 18 to 70 years old (including 18 and 70 years old), both male and female
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Pathologically confirmed advanced malignant tumors that have failed standard treatment or have no effective standard treatment plan
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ECOG score: 0-1
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Expected survival time ≥ 12 weeks
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Existence of measurable lesions that meet RECIST 1.1 standards
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Sufficient Hematology and end organ function shall be completed within 7 days before the first study treatment
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Left ventricular Ejection fraction (LVEF) ≥ 50% within 28 days before the first administration
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Women of childbearing age must carry out serum Pregnancy test within 7 days before the first administration, and the result is negative. Female subjects of childbearing age and male subjects with partners of childbearing age must agree to use efficient methods of contraception or abstinence within at least 26 weeks (female subjects) or 14 weeks (male subjects) from the date of signing the informed consent form until the last administration
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The patient voluntarily joined this study, signed an informed consent form, had good understand the research procedures, and have signed informed consent
Exclusion Criteria:
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Has received treatment with interleukin
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Previously received immune checkpoint inhibitors
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Central nervous system metastasis with clinical symptoms in patients
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The third space effusion with clinical symptoms needs repeated drainage, such as pericardial effusion, Pleural effusion and peritoneal effusion that cannot be controlled after pumping or other treatment
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Subjects who received anti-tumor therapy and systemic immune stimulation therapy within 4 weeks prior to the first dose of the study drug; Received traditional Chinese patent medicines and simple preparations anti-tumor treatment within 2 weeks before the first dose of study drug
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Subjects who received>30Gy of non thoracic radical radiation therapy within 28 days before the first medication, those who received>30Gy of chest radiation therapy within 24 weeks before the first medication, and those who received ≤ 30Gy of palliative radiation therapy within 14 days before the first medication
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Subjects who have received systemic Immunosuppressive drug treatment within 2 weeks before the first administration, or who are expected to require systemic immunosuppressive drug treatment during the study treatment.
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Patients who have not recovered to ≤ CTCAE level 1 (CTCAE v5.0) due to adverse events caused by previous treatment
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Having autoimmune diseases
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Other malignant tumors within 2 years before screening, excluding fully treated cervical Carcinoma in situ, basal cell or squamous cell skin cancer, local prostate cancer after radical surgery, and ductal Carcinoma in situ after radical surgery
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Subjects with known or suspected interstitial pneumonia; Other moderate to severe lung diseases that may interfere with the detection or treatment of drug-related pulmonary toxicity and seriously affect respiratory function
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Subjects with severe cardio cerebral Vascular disease
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Clinically significant bleeding symptoms or tendency to bleed within one month before the first administration
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Arteriovenous thrombotic events that occurred within 3 months before the first administration
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Uncontrolled tumor related pain or symptomatic hypercalcemia. Subjects who require painkillers must already have a stable painkillers treatment plan at the time of entry into the study; Symptomatic lesions suitable for palliative radiotherapy should be treated before entering the study
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Active hepatitis B or active hepatitis C
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Abnormal electrocardiogram (ECG) examination, judged by the researcher to have clinical significance
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Have a history of immune deficiency
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Evidence of active tuberculosis infection within 1 year prior to the first administration, or a history of active tuberculosis infection more than 1 year ago without formal treatment
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Serious infection occurred within 4 weeks before the first administration; Active infections that have received therapeutic intravenous or oral antibiotics within 2 weeks prior to starting the study.
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History of live attenuated vaccine administration within 28 days prior to initial administration or expected study period
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Within 28 days prior to the first administration, major surgeries other than diagnosis or biopsy have been performed; Traumatic minor surgery experienced within 7 days prior to first administration
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Subjects who have previously received or are preparing to receive allogeneic bone marrow transplantation or solid organ transplantation
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Has a history of severe allergic reactions to other monoclonal antibodies/fusion protein drugs, and is allergic to any component of the research treatment plan
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Female subjects during pregnancy, lactation, or planning to conceive during the study period
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The subject has a known history of psychotropic substance abuse, alcoholism, or drug abuse
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Researchers believe that any other medical, psychiatric, or social condition may interfere with the subjects' rights, safety, health, or ability to sign informed consent, cooperate and participate in the study, or interfere with the evaluation of the study medication
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- Suzhou Suncadia Biopharmaceuticals Co., Ltd.
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- SHR-5495-I-101