A Phase I Study to Evaluate the Safety,Tolerability, Pharmacokinetics, and Efficacy of YL211 in Patients With Advanced Solid Tumors

PHASE1RecruitingINTERVENTIONAL
Enrollment

155

Participants

Timeline

Start Date

May 1, 2024

Primary Completion Date

April 7, 2027

Study Completion Date

April 7, 2029

Conditions
Advanced Solid Tumors
Interventions
DRUG

YL211

Patients will be treated with YL211 intravenous (IV) infusion.

Trial Locations (13)

32827

RECRUITING

Sarah Cannon Research Institute at Florida Cancer Specialists, Orlando

75039

RECRUITING

NEXT Oncology - Dallas, Irving

77030

RECRUITING

The University of Texas - MD Anderson Cancer Center, Houston

78229

RECRUITING

NEXT San Antonio, San Antonio

80045

NOT_YET_RECRUITING

University of Colorado Hospital - Anschutz Cancer Pavilion, Aurora

80218-1238

RECRUITING

Sarah Cannon Research Institute (SCRI) at HealthONE, Denver

06473-2142

RECRUITING

Yale School of Medicine - Yale Cancer Center - Smilow Cancer Hospital Care Centers - North Haven, North Haven

34232-6422

RECRUITING

Florida Cancer Specialists & Research Institute (FCS) - Sarasota Cattlemen Office, Sarasota

Unknown

RECRUITING

Monash Health, Melbourne

RECRUITING

Princess Margaret Hospital, Toronto

NOT_YET_RECRUITING

The Ottawa Hospital - General Campus, Ottawa

NOT_YET_RECRUITING

West China Hospital, Sichuan University, Chengdu

RECRUITING

Sun Yat-sen University Cancer Center, Guangzhou

All Listed Sponsors
collaborator

Hoffmann-La Roche

INDUSTRY

lead

MediLink Therapeutics (Suzhou) Co., Ltd.

INDUSTRY