Study of HL-085 in Patients With Advanced Solid Tumor Tumors

PHASE1CompletedINTERVENTIONAL
Enrollment

28

Participants

Timeline

Start Date

December 23, 2020

Primary Completion Date

September 15, 2022

Study Completion Date

December 8, 2022

Conditions
Solid Tumor, Adult
Interventions
DRUG

HL-085

HL-085 is a MEK inhibitor with potential indication for cancers. It will be given twice or three times daily continuously in the study until disease progression; or the risks outweigh the benefits, if the subject continues study treatment; or subjects with poor compliance; or subjects need to receive or have already started alternative antitumor drugs; or Subjects who need to receive or have already started alternative any other concomitant medication and/or treatment, which would significantly impact their safety; or interruption of IP administration for more than 14 days due to IP-related AEs.

Trial Locations (5)

37203

SCRI, Nashville

44718

Gabrail Cancer Center, Canton

77030

Oncology Consultants, Houston

89169

Comprehensive Cancer Centers, Las Vegas

92069

CCARE, San Marcos

Sponsors
All Listed Sponsors
lead

Kechow Pharma, Inc.

INDUSTRY