To Explore the Efficacy and Safety of Camrelizumab Combined With SHR1020 in the Treatment of Advanced Melanoma

NCT ID: NCT05051865

Last Updated: 2022-11-17

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-10-09
• Study Completion Date: 2024-08-30

Brief Summary

This study is being conducted to explore the efficacy and safety of camrelizumab combined with SHR1020 in the treatment of advanced melanoma.

Detailed Description

This trial is a prospective, single-center, single-arm clinical research. Based on current experience, single agent immunotherapy has limited efficacy in advanced melanoma. SHR1020 is a multi-target tyrosine kinase inhibitor. This study is aiming to evaluate the efficacy and safety of camrelizumab combined with SHR1020 in patients with advanced melanoma. The safety and efficacy of this study will be assessed through ORR, DCR, PFS, OS and adverse effects as graded by CTCAE 5.0.

Conditions

Melanoma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Camrelizumab Combined With SHR1020

Camrelizumab combined with SHR1020 for advanced melanoma.

Group Type: EXPERIMENTAL

camrelizumab

Intervention Type: DRUG

camrelizumab combined with SHR1020 for advanced melanoma

SHR1020

Intervention Type: DRUG

camrelizumab combined with SHR1020 for advanced melanoma

Interventions

camrelizumab

camrelizumab combined with SHR1020 for advanced melanoma

Intervention Type: DRUG

SHR1020

camrelizumab combined with SHR1020 for advanced melanoma

Intervention Type: DRUG

Other Intervention Names

SHR1210

Eligibility Criteria

Inclusion Criteria

• Has unresectable Stage III or Stage IV melanoma per American Joint Committee on Cancer (AJCC) staging system version 8. At least one measurable lesion conforming to RECIST 1.1 criteria.
• The toxicity of prior treatment has recovered to ≤1 grade according to CTCAE 5.0 (excepted alopecia).
• ECOG score 0-1.
• The expected survival time is ≥ 12 weeks.
• Had normal swallowing function, without dysfunction of gastrointestinal absorption.
• Adequate organ and bone marrow function.
• Female patients of childbearing age must undergo a serum pregnancy test within 7 days before the commencement of the study and the results are negative, and are willing to use a medically approved high potency contraceptive method during the study period and within 12 months after the last administration of the study drug; For male patients whose partner is a female of childbearing age, they should be surgically sterilized or agree to use an effective method of contraception during the study period and for 12 months after administration of the last study.
• Willing to consent and signed the informed consent, and able comply with the planned visit, research treatment, laboratory examination and other test procedures.

Exclusion Criteria

• Other malignant tumors occurred in the past 5 years, except for cured skin basal cell carcinoma, squamous cell carcinoma of skin, early stage prostate cancer and cervical carcinoma in situ.
• Has uveal melanoma.
• The patient has previously received anti-angiogenic drugs.
• The first study drug treatment was less than 4 weeks from the last chemotherapy or 5 half-lives from the last targeted therapy; less than 4 weeks from major surgery; less than7 days from immunosuppressive drug; less than 3 weeks from immunomodulatory; less than 4 weeks from live attenuated vaccine.
• Systemic antibiotic use for 7 days within 4 weeks prior to initial administration, or unexplained fever during screening/prior to initial administration.
• Received hematopoietic stimulating factors (eg: G-CSF, EPO) within 1 week prior to initial administration.
• Patients with central nervous system disease or brain metastases; patients who have received treatment, such as imaging confirmed stable has been maintained for at least 4 weeks, and have stopped systemic hormone therapy for more than 2 weeks, no clinical symptoms can be included.
• With active autoimmune disease or a history of autoimmune disease.
• With history of allogeneic organ transplantation or allogeneic hematopoietic stem cell transplantation.
• With immunodeficiency, eg HIV, HBV, HCV.
• Known to be allergic to the active ingredients or excipients in this study.
• Have a clear history of serious and uncontrolled other disease or mental disorders.
• Has a bleeding tendency or abnormal clotting function (INR>2.0, PT>16s).
• Other situations that the researcher considers inappropriate to participate in the research.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Peking University Cancer Hospital & Institute

OTHER

Sponsor Role: lead

Responsible Party

Jun Guo

Clinical Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Jun Guo, MD

Role: PRINCIPAL_INVESTIGATOR

Peking University Cancer Hospital & Institute

Locations

Beijing Cancer Hospital

Beijing, Beijing Municipality, China

Site Status: RECRUITING

Countries

China

Central Contacts

Lili Mao, MD

Role: CONTACT

yunzhongmanbu7848@163.com

13261859885

Jun Guo, MD

Role: CONTACT

Facility Contacts

Jun Guo, MD

Role: primary

guoj307@126.com

+861088196348

Other Identifiers

MM-IIT-SHR1210-FMTN

Identifier Type: -

Identifier Source: org_study_id