A Phase I/II Trial of the MUC1 Inhibitor, GO-203-2C in Patients With Relapsed or Refractory Acute Myeloid Leukemia

Recurrent Adult Acute Myeloid Leukemia Clinical Trial

Official title:

A Phase I/II Trial of the MUC1 Inhibitor, GO-203-2C in Patients With Relapsed or Refractory Acute Myeloid Leukemia

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT02204085
• Other study ID #: 14-222
• Status: Active, not recruiting
• Phase: Phase 1/Phase 2
• Start date: September 2014
• Est. completion date: December 2024

Study information

• Verified date: June 2024
• Source: Beth Israel Deaconess Medical Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This research study is studying a targeted therapy known as GO-203-2C as a possible treatment for with acute myeloid leukemia (AML) both alone and in combination with decitabine. GO-203-2c targets cancer cells, while leaving healthy cells unaffected.This is a Phase I/II clinical trial. A Phase I clinical trial tests the safety of an investigational intervention and also tries to define the appropriate dose of the investigational intervention to use for further studies.

Description:

• Phase I

• The maximum tolerated dose (MTD) will be determined in the phase I section of the trial.

• Patients who fulfill eligibility criteria will be entered into the trial to GO-203-2c.

• After the screening procedures confirm participation in the research study. The investigators are looking for the highest dose of the combination of study drugs that can be administered safely without severe or unmanageable side effects in participants that have acute myeloid leukemia (AML) not everyone who participates in this research study will receive the same dose of the study drug. The dose given will depend on the number of participants who have been enrolled in the study prior and how well the dose was tolerated.

• A subsequent dose escalation will evaluate the combination of GO-203-2c and decitabine.

• Phase II

• The primary goal is to determine if the combination of the two drugs results in clinical response

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 33
• Est. completion date: December 2024
• Est. primary completion date: September 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• To be considered eligible for enrollment into this study, all of the following inclusion criteria must be met during the screening period:

• Documented AML by peripheral blood and bone marrow analyses meeting WHO criteria, excluding patients with acute promyelocytic leukemia (APL)

• Patients with AML refractory to primary induction chemotherapy, relapsed disease, or age = 60 and not appropriate for standard cytotoxic therapy due to age, performance status, and/or adverse risk factors according to the treating physician

• Age = 18 years

• Karnofsky performance status = 50% or ECOG performance status 0-2

• Life expectancy = 6 weeks

• Able to understand the investigational nature of this study and to provide written consent to participate in it

• Signed written IRB-approved Informed Consent document

• Adequate hepatic and renal function:

• serum bilirubin = 1.5 X institutional ULN OR serum direct bilirubin = 2 X institutional ULN

• serum ALT and AST = 2.5 X institutional ULN

• serum alkaline phosphatase < 5 X institutional ULN

• serum creatinine = 2.0 mg/dL

• corrected calcium level = institutional LLN

• Negative pregnancy test in women of child-bearing potential

• Women and men of child-producing potential must agree to use effective contraceptive methods during the study period (including post-treatment observation period)

Exclusion Criteria:

• A patient will be considered not eligible for enrollment into this study if any of the following criteria are met during the screening period:

• Evidence of leukemic meningitis or other CNS involvement by leukemia

• Uncontrolled or poorly controlled hypertension (systolic BP = 160 mmHg or diastolic BP = 100 mmHg) Note: an isolated reading that is not sustained will be permitted.

• Evidence of NYHA Class III or IV cardiac disease, or presence of unstable life-threatening arrhythmia, or history of myocardial infarction during the past 6 months

• Active bacterial, fungal, or viral infection requiring systemic treatment

• Known infection with HIV

• History or major surgery within 4 weeks before the first dose of study treatment, or not recovered from prior surgery

• Exposure to any other investigational agent at any time within 4 weeks before the first dose of study treatment

• Exposure to any other anti-leukemic therapy (except hydroxyurea, see Section 5.5.1) within 2 weeks before the first dose of study treatment

• Pregnant or lactating female

• Unwilling or unable to comply with the requirements of the study protocol

Related Conditions & MeSH terms

• Acute Myeloid Leukemia, in Relapse
• Leukemia
• Leukemia, Myeloid
• Leukemia, Myeloid, Acute
• Recurrent Adult Acute Myeloid Leukemia

Intervention

Drug:
• GO-203-2c

• GO-203-2c + Decitabine

Locations

Country	Name	City	State
United States	Beth Israel Deaconess Medical Center	Boston	Massachusetts
United States	Dana-Farber Cancer Institute	Boston	Massachusetts

Sponsors (2)

Lead Sponsor	Collaborator
Beth Israel Deaconess Medical Center	Dana-Farber Cancer Institute

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maximum Tolerated Dose of GO-203-2c	Phase I	28 days
Primary	Maximum Tolerated Dose of GO-203-2c in combination with decitabine	Phase 1	28 days
Secondary	Number of Participants with Adverse Events as a Measure of Safety and Tolerability		2 years
Secondary	To investigate whether GO-203-2c alone and in combination with decitabine is effective in targeting MUC1-C overexpressing AML progenitor cells in the lab		2 Years
Secondary	To assess whether in vitro response to GO-203-2c alone and in combination with decitabine is associated with clinical response		2 Years
Secondary	To determine if therapy with GO-203-2c alone and in combination with decitabine results in decreased engraftment potential of AML progenitor cells in an NSG mouse model		2 Years
Secondary	To determine if therapy GO-203-2c in combination with decitabine results in at least 20% of patients achieving a clinical response	To determine if therapy GO-203-2c in combination with decitabine results in at least 20% of patients achieving a clinical response (blast response, minor response, partial response, or complete response).	2 years