KPG-818 (Blood, Bone Marrow, and Lymph Node Cancers)

Purpose of this Study

We are doing this study to find out if an experimental drug called KPG-818 (the study drug) is a safe and effective treatment for various hematological malignancies. The study drug will be combined with dexamethasone for participants who have multiple myeloma.

Who Can Participate?

Eligibility

Adults diagnosed with hematological malignancies who:
  • Have relapsed from previous treatment; OR
  • Did not have an adequate response to standard treatments; OR
  • Have not received treatment yet
For more information about who can join this study, please contact the study team at 919-684-9220.

What is Involved?

Description

If you choose to join this study, you will go through a screening period to find out if you are eligible. During this screening period, you will:
  • Have a physical exam
  • Have a heart scan (ECG)
  • Have blood draws and give urine samples
  • Have bone marrow samples taken
  • Have images taken (X-ray or CT scan)
After screening, this study is divided into 2 different parts, Part 1 and Part 2:
  • During Part 1, increasing doses of the study drug will be given to participants who have certain hematological malignancies
  • During Part 2, a fixed dose of the study drug will be given to participants who have certain hematological malignancies based on the results of Part 1
The study drug period for Part 1 and Part 2 will consist of drug cycles, which will be 28 days. Subjects will take the study drug on Days 1 to 21 of each cycle (i.e., you will take the drug every day for 3 weeks, followed by 1 week of not taking the drug).
  • During the first study drug cycle, you will have 4 visits
  • Cycle 2 will have 4 visits
  • Cycles 3 and onward will have 1 visit
More than 6 cycles of study drug will be allowed if you do not meet any stopping rules at the end of the first 6 cycles of study drug, and if you and your study doctor believe that you are benefiting from the study drug. Once you stop taking the study drug, we will schedule you for a series of follow-up visits to see how you are doing.

Study Details

Full Title

A Phase 1, Multicenter, Open-label, Multiple-ascending Dose Study to Evaluate the Safety, Pharmacokinetics and Clinical Activity of KPG-818 in Subjects with Hematological Malignancies

Principal Investigator

Cristina
Gasparetto

Protocol Number

PRO00107334

NCT ID

NCT04643067

Phase

I

Enrollment Status

Open to Enrollment