A Phase Ib/II Study of AK104 and AK117 in Combination With or Without Chemotherapy in Advanced Malignant Tumors

NCT05235542 · Status: UNKNOWN · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 130

Last updated 2022-08-11

No results posted yet for this study

Summary

Phase Ib/II open label, multicenter study to evaluate the efficacy and safety of AK104 (anti-PD-1 and CTLA-4 bispecific antibody) and AK117#AntiCD47 Antibody# combined with or without chemotherapy in advanced malignant tumors

Conditions

  • Advanced Malignant Tumors

Interventions

DRUG

AK104

IV infusion,Specified dose on specified days

DRUG

AK117

IV infusion,Specified dose on specified days

DRUG

Capecitabine tablets

Oral,Specified dose on specified days

DRUG

Oxaliplatin

IV infusion,Specified dose on specified days

DRUG

Cisplatin

IV infusion,Specified dose on specified days

DRUG

Paclitaxel

IV infusion,Specified dose on specified days

DRUG

Irinotecan

IV infusion,Specified dose on specified days

DRUG

Docetaxel

IV infusion,Specified dose on specified days

DRUG

5-FU

IV infusion,Specified dose on specified days

Sponsors & Collaborators

Principal Investigators

  • Liwei Wang, MD · RenJi Hospital

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-07-12
Primary Completion
2023-03-31
Completion
2024-03-31

Countries

  • China

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05235542 on ClinicalTrials.gov