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Clinical Trials/NCT04245397
NCT04245397
Recruiting
Phase 1

A Phase 1, Open-Label, Dose-Escalation With Expansion Study of SX-682 Alone and in Combination With Oral or Intravenous Decitabine in Subjects With Myelodysplastic Syndrome

Syntrix Biosystems, Inc.7 sites in 1 country151 target enrollmentJune 30, 2020

Overview

Phase
Phase 1
Intervention
SX-682
Conditions
Myelodysplastic Syndromes
Sponsor
Syntrix Biosystems, Inc.
Enrollment
151
Locations
7
Primary Endpoint
SX-682 Maximum Tolerated Dose (MTD)
Status
Recruiting
Last Updated
4 months ago

Overview

Brief Summary

This study will determine the safety profile, maximum tolerated dose (MTD), dose-limiting toxicities (DLT), and recommended Phase 2 dose (RP2D) of SX-682 in the treatment of patients with Myelodysplastic Syndromes (MDS).

Detailed Description

Participants will receive twice daily oral SX-682 for six 28 day cycles. If patients are responding well to the treatment they can continue SX-682 treatment. The first participants will be administered 25 mg orally twice daily. Unless dose limiting toxicities occur, participants will enroll and receive the following increasing twice daily doses of SX-682: 50 mg, 100 mg, 200 mg, and 400 mg. After establishing the maximum tolerated dose 140 additional participants will be enrolled at the recommended phase 2 dose. Participants will receive continuous SX-682 twice daily oral therapy in 28-day cycles for a total of 6 cycles. The expansion dose cohort will be stratified into IPSS (a) low and intermediate-1 (N=20 SX-682 alone in HMA naive, N=20 SX-682 alone in HMA failure, N=20 SX-682 + DEC-C in HMA-naïve, N=20 SX-682 + DEC-C in HMA-failure) and (b) intermediate-2 and high risk (N=20 SX-682 alone in HMA failure, N=20 SX-682 + DEC-C in HMA-naive, N=20 SX-682 + DEC-C in HMA-failure) MDS. For patients responding well at the end of 6 cycles treatment may continue until disease progression or an adverse event leads to SX-682 discontinuation. Except for blood product transfusions, concurrent therapy for Myelodysplastic Syndromes is not permitted.

Registry
clinicaltrials.gov
Start Date
June 30, 2020
End Date
March 1, 2029
Last Updated
4 months ago
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of MDS by World Health Organization criteria, and either
  • International Prognostic Scoring System (IPSS) low risk or intermediate-1 risk patients without 5q deletion:
  • i. Dose escalation portion: failed prior treatment with at least 4 cycles started of a hypomethylating agent (HMA; azacitidine or decitabine) defined as no response to treatment, loss of response at any time point, or progressive disease/intolerance to therapy.
  • ii. Dose expansion portion: failed prior treatment defined as no response to treatment with at least 4 cycles started of HMA, loss of response at any time point, or progressive disease/intolerance to therapy ("HMA failure"); or no prior treatment with HMA ("HMA naive").
  • IPSS low risk or intermediate-1 risk patients with 5q deletion:
  • i. Dose escalation portion: failed prior treatment with at least 4 cycles started of lenalidomide and 4 cycles of hypomethylating agent (azacitidine or decitabine) defined as no response to treatment, loss of response at any time point, or progressive disease/intolerance to therapy.
  • ii. Dose expansion portion: same as non-del(5q) lower risk cohort + requirement of failed prior treatment with lenalidomide defined as no response to treatment with at least 4 cycles started of lenalidomide, loss of response at any time point, or progressive disease/intolerance to therapy.
  • IPSS intermediate-2 risk or high risk patients: HMA failure or HMA naïve as defined above.
  • Eastern Cooperative Oncology Group (ECOG) Performance Status ≤ 2
  • Screening laboratory values:

Exclusion Criteria

  • Use of chemotherapeutic agents or experimental agents for MDS within 14 days of the first day of study drug treatment.
  • Use of erythroid stimulating agents, Granulocyte-colony stimulating factor (G-CSF), or Granulocyte-macrophage colony-stimulating factor (GM-CSF) within 14 days of the first day of study drug treatment, or during the study.
  • Mean triplicate heart rate-corrected QT interval (QTc) \> 500 msec.
  • Any of the following cardiac abnormalities:
  • QT interval \> 480 msec corrected using Fridericia's formula;
  • Risk factors for Torsade de Pointes;
  • Use of medication that prolongs the QT interval with the exception of drugs that are considered absolutely essential for the care of the subject;
  • Myocardial infarction ≤ 6 months prior to first day of study drug treatment;
  • Unstable angina pectoris or serious uncontrolled cardiac arrhythmia.
  • Any serious or uncontrolled medical disorder.

Arms & Interventions

Dose Escalation of SX-682

Escalating oral doses of SX-682 (study drug) of 25, 50, 100, 200 and 400 mg twice-daily (i.e., 50, 100, 200, 400 and 800 mg total each day.

Intervention: SX-682

Expansion of SX-682 alone (lower risk patients, naive to hypomethylating agents)

Expansion of oral doses of SX-682 (study drug) at 200 mg twice daily (recommended phase 2 dose) in lower risk patients who have never received hypomethylating agents.

Intervention: SX-682

Expansion of SX-682 alone (lower risk patients, failed on hypomethylating agents)

Expansion of oral doses of SX-682 (study drug) at 200 mg twice daily (recommended phase 2 dose) in lower risk patients who failed on hypomethylating agents.

Intervention: SX-682

Expansion of SX-682 with decitabine (lower risk patients, naive to hypomethylating agents)

Expansion of oral doses of SX-682 (study drug) at 100 mg twice daily with decitabine in lower risk patients who have never received hypomethylating agents.

Intervention: SX-682

Expansion of SX-682 with decitabine (lower risk patients, naive to hypomethylating agents)

Expansion of oral doses of SX-682 (study drug) at 100 mg twice daily with decitabine in lower risk patients who have never received hypomethylating agents.

Intervention: Decitabine

Expansion of SX-682 with decitabine (lower risk patients, failed on hypomethylating agents)

Expansion of oral doses of SX-682 (study drug) at 100 mg twice daily with decitabine in lower risk patients who failed on hypomethylating agents.

Intervention: SX-682

Expansion of SX-682 with decitabine (lower risk patients, failed on hypomethylating agents)

Expansion of oral doses of SX-682 (study drug) at 100 mg twice daily with decitabine in lower risk patients who failed on hypomethylating agents.

Intervention: Decitabine

Expansion of SX-682 alone (higher risk patients, failed on hypomethylating agents)

Expansion of oral doses of SX-682 (study drug) at 200 mg twice daily (recommended phase 2 dose) in higher risk patients who failed on hypomethylating agents.

Intervention: SX-682

Expansion of SX-682 with decitabine (higher risk patients, naive to hypomethylating agents)

Expansion of oral doses of SX-682 (study drug) at 100 mg twice daily with decitabine in higher risk patients who have never received hypomethylating agents.

Intervention: SX-682

Expansion of SX-682 with decitabine (higher risk patients, naive to hypomethylating agents)

Expansion of oral doses of SX-682 (study drug) at 100 mg twice daily with decitabine in higher risk patients who have never received hypomethylating agents.

Intervention: Decitabine

Expansion of SX-682 with decitabine (higher risk patients, failed on hypomethylating agents)

Expansion of oral doses of SX-682 (study drug) at 100 mg twice daily with decitabine in higher risk patients who failed on hypomethylating agents.

Intervention: SX-682

Expansion of SX-682 with decitabine (higher risk patients, failed on hypomethylating agents)

Expansion of oral doses of SX-682 (study drug) at 100 mg twice daily with decitabine in higher risk patients who failed on hypomethylating agents.

Intervention: Decitabine

Outcomes

Primary Outcomes

SX-682 Maximum Tolerated Dose (MTD)

Time Frame: Up to 28 days in the 28 day Cycle 1.

Participants cohorts will be enrolled at increasing doses of SX-682. The highest SX-682 dose tested at which no more than 1 of 6 participants experiences a dose limiting toxicity will define the SX-682 MTD

SX-682 Dose Limiting Toxicities (DLT)

Time Frame: Up to 28 days in the 28 day Cycle 1.

Number of participants experiencing DLTs.

Secondary Outcomes

  • Participants Experiencing a Treatment Response(At the end of Cycle 6 (each cycle is 28 days).)
  • SX-682 Steady-State Minimum Plasma Concentration (Css min)(Day 15 of Cycle 1 (each cycle is 28 days).)
  • SX-682 Single Dose Maximum Plasma Concentration (Cmax)(Day 1 of Cycle 1 (each cycle is 28 days).)
  • SX-682 Delayed Dose Limiting Toxicities(From the beginning of Cycle 2 to the end of Cycle 6 (each cycle is 28 days).)
  • SX-682 Steady-State Maximum Plasma Concentration (Css max)(Day 15 of Cycle 1 (each cycle is 28 days).)
  • Adverse Events(At the end of Cycle 6 (each cycle is 28 days).)

Study Sites (7)

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