IBI188 Combination Therapy in Solid Tumors

NCT04861948 · Status: TERMINATED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 9

Last updated 2022-10-04

No results posted yet for this study

Summary

A Phase Ib study aim to evaluate the efficacy, safety, and tolerability of IBI188 combination therapy in subjects with advanced malignancies

Conditions

Interventions

DRUG

IBI188

intravenous

DRUG

GM-CSF

subcutaneous injection

DRUG

Cisplatin/Carboplatin

intravenous

DRUG

Bevacizumab

intravenous

DRUG

Sintilimab

intravenous

DRUG

Pemetrexed

intravenous

Sponsors & Collaborators

  • Innovent Biologics (Suzhou) Co. Ltd.

    lead INDUSTRY

Principal Investigators

  • Ba Yi · Tianjin Medical University Cancer Institute and Hospital

  • Zhang Dahong · Zhejiang Provincial People's Hospital

  • Guo Hongqian · The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School

  • Fang Meiyu · Zhejiang Cancer Hospital

  • Xie Yu · Hunan Cancer Hospital

  • Liu Jisheng · First Affiliated Hospital of Soochow University

  • Wang Ying · Zhejiang Provincial People's Hospital

  • Wang Haiying · Shougang Hospital, Peking University

  • Wang Mengzhao · Shougang Hospital, Peking University

  • Lv Qiang · Jiangsu Provincial People's Hospital

  • Li Xiangping · Nanfang Hospital, Southern Medical University

  • Liu Guihong · The Affiliated Hospital of Xuzhou Medical University

  • Mou Weiqi · Chongqing University Cancer Hospital

  • Guo Wei · Peking Union Medical College

  • Wang Wei · Hunan Cancer Hospital

  • Xu Chongyuan · Nanfang Hospital, Southern Medical University

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
12 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-05-25
Primary Completion
2022-07-30
Completion
2022-07-30

Countries

  • China

Study Locations

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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 NCT04861948 on ClinicalTrials.gov