Overview

PD-1 Antibody SHR-1210 Combined With Apatinib of First-line Treatment of Advanced Acral Melanoma

Status:
Unknown status
Trial end date:
2021-04-10
Target enrollment:
0
Participant gender:
All
Summary
the investigators launched this exploratory study to evaluate the objective response rate (ORR) of SHR-1210 combined with apatinib mesylate in the first-line treatment of patients with advanced acral melanoma.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Beijing Cancer Hospital
Treatments:
Antibodies
Apatinib
Criteria
Inclusion Criteria:

1. age:18-75 years, male or female.

2. Histopathologically confirmed recurrence, inoperable resection or metastatic acral
melanoma (stage III/IV).

3. Has not received any systematic anti-tumor drug treatment.

4. Measurable disease based on Response Evaluation Criteria In Solid Tumors (RECIST) 1.1.

5. ECOG 0-1.

6. Adequate organ function.

7. Life expectancy of greater than 12 weeks.

8. Patient has given written informed consent.

Exclusion Criteria:

1. Patients who have or are currently undergoing additional chemotherapy, radiation
therapy, targeted therapy or immunotherapy.

2. Known history of hypersensitivity to macromolecular protein preparation or any
components of the SHR- 1210 formulation.

3. Subjects before or at the same time with other malignant tumors (except which has
cured skin basal cell carcinoma and cervical carcinoma in situ);

4. Subjects with any active autoimmune disease or history of autoimmune disease

5. Uncontrolled clinically significant heart disease, including but not limited to the
following: (1) > NYHA II congestive heart failure; (2) unstable angina, (3) myocardial
infarction within the past 1 year; (4) clinically significant supraventricular
arrhythmia or ventricular arrhythmia requirement for treatment or intervention;

6. Active infection or an unexplained fever > 38.5°C during screening or before the first
scheduled day of dosing (subjects with tumor fever may be enrolled at the discretion
of the investigator);

7. Received a live vaccine within 4 weeks of the first dose of study medication.

8. Pregnancy or breast feeding.

9. Decision of unsuitableness by principal investigator or physician-in charge.