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Study details
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A Study of an MMSET Inhibitor in Patients With Relapsed and Refractory Multiple Myeloma

K36 Therapeutics, Inc.
NCT IDNCT05651932ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

125

Study length

about 3.4 years

Ages

18+

Locations

13 sites in CA, FL, GA +8

About this study

Researchers are testing a new drug called KTX-1001 to see if it's safe for people with multiple myeloma that has returned or not responded to other treatments. The trial will involve different groups of patients receiving varying combinations of the drug, including KTX-1001 alone and in combination with other medications like mezigdomide, carfilzomib, or pomalidomide.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take Cohort A1 & A2: KTX-1001
  • 2.Take Cohort B1 & B2: KTX-1001+Mezigdomide
  • 3.Take Cohort C1 & C2: KTX-1001 + Carfilzomib (KYPROLIS®)
  • +1 more
PhasePhase 1
DrugCarfilzomib (KYPROLIS®)
Routeinjection
Primary goalDose Escalation: Determination of Recommended Phase 2 Dose (RP2D) and/or Maximum Tolerated Dose (MTD) Dose Expansion: Provide preliminary efficacy data on the antitumor effects of KTX-1001 in combination with other anti-myeloma therapy

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low6%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Drug classes

carfilzomib, pomalidomide

Drug routes

injection (Injection), oral (Oral Capsule)

Endpoints

Primary: Dose Escalation: Determination of Recommended Phase 2 Dose (RP2D) and/or Maximum Tolerated Dose (MTD) Dose Expansion: Provide preliminary efficacy data on the antitumor effects of KTX-1001 in combination with other anti-myeloma therapy

Secondary: Pharmacokinetics & Pharmacodynamics KTX-1001± Combination Therapy

Body systems

Oncology