Safety, Tolerability and Pharmacokinetics Study of KPG-818 in Hematological Malignancies Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

September 13, 2021

Primary Completion Date

December 12, 2024

Study Completion Date

December 12, 2024

Conditions
Hematological Malignancies
Interventions
DRUG

KPG-818

The 4 planned dose level (cohorts) of KPG-818 will be explored: 2, 3, 4 and 5mg. Each dose of KPG-818 will be administered orally with approximately 240 ml of water daily, and used as a single agent in subjects with selected hematological malignancies (or in combination with dexamethasone weekly for MM), according to specific dosing schedule in each treatment cycle until disease progression, unacceptable toxicity, the subject withdraws, or any other study withdrawal criterion is met. The treatment of study is divided into 6 cycles.

Trial Locations (10)

15232

UPMC CancerCenter, Pittsburgh

33322

BRCR Global - USA, Plantation

40202

Norton Cancer Institute, Louisville

78041

Laguna Clinical Research Associates, Laredo

95817

UC Davis Comprehensive Cancer Center, Sacramento

97213

Providence Portland Medical Center, Portland

48202-2689

Henry Ford Health System - Hemophilia and Thrombosis Treatment Center, Detroit

07960

Mohamad Medical Cherry, Morristown

27710-4000

Duke University Health System - Duke Endoscopy - Duke Clinic 2H, Durham

53226-0509

Medical College of Wisconsin, Milwaukee

All Listed Sponsors
lead

Kangpu Biopharmaceuticals, Ltd.

INDUSTRY

NCT04283097 - Safety, Tolerability and Pharmacokinetics Study of KPG-818 in Hematological Malignancies Subjects | Biotech Hunter | Biotech Hunter