Birinapant With 5-azacitidine in MDS Subjects Who Are Naïve, Have Relapsed or Are Refractory to 5-azacitidine Therapy

Myelodysplastic Syndrome Clinical Trial

Official title:

A Phase 1b/2a, Open-label, Non-randomized Study of Birinapant in Combination With 5-azacitidine in Subjects With Myelodysplastic Syndrome Who Are Naïve, Refractory or Have Relapsed to 5-azacitidine Therapy

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01828346
• Other study ID #: TL32711-0087
• Status: Completed
• Phase: Phase 1/Phase 2
• First received: April 5, 2013
• Last updated: April 19, 2016
• Start date: June 2013
• Est. completion date: November 2015

Study information

• Verified date: April 2016
• Source: TetraLogic Pharmaceuticals
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

This is a dose escalation followed by dose expansion study of TL32711 in combination with 5-Azacitidine in subjects with Myelodysplastic syndrome who are naïve, have relapsed or have failed prior 5-azacitidine therapy. Pre-clinical and mechanistic studies support that 5-Azacitidine may modulate pathways that enable birinapant-mediated anti-tumor activity.

Description:

This is a Phase 1b/2a, open-label, non-randomized study in male and female subjects with MDS who are naïve, refractory or have relapsed to 5-Azacitidine therapy.

Primary Objective is to determine the maximum tolerated dose (MTD), recommended Phase 2 dose, and pharmacodynamics (PD) of birinapant (TL32711) when administered in combination with 5-azacitidine (5 AZA) in subjects with myelodysplastic syndrome (MDS) who are naïve, refractory or have relapsed to 5-AZA therapy.

Secondary Objectives are to determine the clinical activity using the International Working Group (IWG) (Cheson, 2006) Response Criteria for MDS during the Phase 1b dose escalation stage of the study and in the Phase 2a expansion cohort, to determine the pharmacokinetics (PK) of birinapant when administered with 5-AZA in plasma and to assess exploratory translational biomarkers of anti-tumor activity of birinapant in combination therapy.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 21
• Est. completion date: November 2015
• Est. primary completion date: June 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Men or women more than 18 years of age.

• Patients with high-risk Myelodysplastic Syndrome

• Performance status of greater or equal to 2 by the Eastern Cooperative Oncology Group (ECOG) scale.

• Subjects with high-risk MDS who are naïve to 5-Azacitidine or have previously received 5-AZA or decitabine as first-line cytotoxic therapy. Subjects with prior 5-Azacitidine therapy were evaluated to be either refractory or relapsed as determined by the Investigator, according to IWG response criteria.Subjects with relapsed or refractory disease may have only received prior 5-Azacitidine or decitabine.

• Hydroxyurea for patients with rapidly proliferative disease can be used up to 24 hours prior to therapy but not concomitantly with 5-Azacitidine.

• Adequate liver, pancreatic and renal function.

• Women of childbearing potential must have a negative serum pregnancy test at screening within 48 hours prior to the first dose

• Women of childbearing potential must agree to use 2 methods of adequate contraception

Exclusion Criteria:

• Subjects with life-threatening toxicity or non tolerability to prior 5-Azacitidine therapy.

• Subjects with hypoplastic Myelodysplastic syndrome.

• Subjects with >30% bone marrow blast cells.

• Subjects with malignant hepatic tumors or secondary malignancy within 2 years

• Known diagnosis of human immunodeficiency virus or chronic active Hepatitis B or C.

• Uncontrolled hypertension

• Impaired cardiac function, uncontrolled cardiac arrhythmias despite medications,

• QT interval corrected for heart rate (QTcB) more than 480 msec

• Lack of recovery of prior adverse events to Grade =1 severity (National Cancer Institute Common Terminology Criteria for Adverse Events version 4) (except alopecia) due to therapy administered prior to the initiation of study drug dosing.

• Nursing or pregnant women.

• Known allergy to any of the formulation components of birinapant.

• Known or suspected hypersensitivity to 5-Azacitidine or mannitol.

• Any concurrent disease and/or medical condition that, in the opinion of the Investigator, would prevent the subject's participation.

• History of Bell's Palsy.

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Myelodysplastic Syndrome
• Myelodysplastic Syndromes
• Preleukemia

Intervention

Drug:
• Birinapant
Dose escalation part: (Drug escalation dose levels) Dose Level (1) - 13mg/m2 (twice a week for 3 of 4 weeks) Dose Level (-1) - 11 mg/m2 (twice a week for 3 of 4 weeks) Dose Level (2) - 13mg/m2 (twice weekly x 4 weeks) Dose Level (3a) - 17mg/m2 (twice weekly × 4 weeks)OR Dose Level (3b) - 17mg/m2 (twice a week for 3 of 4 weeks)
• 5-Azacitidine
Dose Level (0) - 75mg/m2 daily

Locations

Country	Name	City	State
United States	Roswell Park Cancer Institute	Buffalo	New York
United States	California Cancer Associates for Research and Excellence	Fresno	California
United States	Palo Verde Hematology Oncology	Glendale	Arizona
United States	The University of Texas M.D. Anderson Cancer Center	Houston	Texas
United States	Mayo Clinic Jacksonville	Jacksonville	Florida
United States	University of Pennsylvania, Abramson Cancer Center	Philadelphia	Pennsylvania
United States	Mayo Clinic Scottsdale	Scottsdale	Arizona

Sponsors (1)

Lead Sponsor	Collaborator
TetraLogic Pharmaceuticals

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maximum tolerated dose (MTD)		6 months	Yes