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Spots Global Cancer Trial Database for Study of AK119 and AK 112 With or Without Chemotherapy for Colorectal Cancer Patients

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Trial Identification

Brief Title: Study of AK119 and AK 112 With or Without Chemotherapy for Colorectal Cancer Patients

Official Title: A Phase Ib/II Study of AK112 and AK119 in Combination With or Without Chemotherapy in the Treatment of Patients With Advanced Microsatellite Stabilized (pMMR/MSS) Colorectal Cancer

Study ID: NCT05846867

Study Description

Brief Summary: This is a phase Ib/II clinical study on AK119 and AK112 combined with or without chemotherapy in advanced microsatellite stabilized (pMMR/MSS) colorectal cancer

Detailed Description: The study included the screening period (no more than 28 days after the subject signed the informed consent form to the first medication), the treatment period (until the investigator assessed that there was no clinical benefit, intolerable toxicity or withdrew the informed consent, whichever occurred first) and the follow-up period (including safety follow-up, disease progress follow-up and survival follow-up). Subjects will be screened and evaluated within 28 days before the first medication to determine whether they meet the study conditions. During the screening period, tumor samples of the subjects need to be collected. Subjects who meet the study conditions will be treated according to the study medication plan until the following conditions occur: the investigator judges that the subject cannot continue to benefit, there is intolerable toxicity, there is a concomitant disease that affects further treatment, the investigator decides, the subject withdraws his informed consent or the treatment needs to be terminated for other reasons specified in the plan (whichever occurs first). The investigator regularly evaluated the tumor response of all subjects according to RECIST 1.1 standard. Subjects were evaluated once every 6 weeks (± 7 days) within 54 weeks after enrollment, and then once every 9 weeks (± 7 days). For subjects undergoing treatment, their clinical decisions are based on the tumor response evaluated by the researchers

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Cancer Hospital Affiliated to Harbin Medical University, Harbin, , China

Contact Details

Name: Yanqiao Zhang, PhD

Affiliation: Cancer Hospital Affiliated to Harbin Medical University

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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