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Clinical Trials/NCT05519527
NCT05519527
Withdrawn
Phase 1

A Phase 1 Study of Safety and Efficacy of an Anti-CD38 Antibody Drug Conjugate (STI-6129) in Patients With Relapsed or Refractory T-Acute Lymphoblastic Leukemia/Lymphoma (T-ALL) or Acute Myeloid Leukemia (AML)

M.D. Anderson Cancer Center0 sitesStarted: August 16, 2022Last updated:

Overview

Phase
Phase 1
Status
Withdrawn
Primary Endpoint
Severity of the adverse events (Aes) -The severity of the adverse events (Aes) will be graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) V.5

Overview

Brief Summary

This is an open-label, phase 1b/2 trial. It is designed to identify the recommended phase 2 dose (RP2D) of STI-6129, and the safety and efficacy of this anti-CD38-Duostatin 5.2 antibody-drug conjugate (ADC) for the treatment of R/R T-ALL and AML who have exhausted standard of care treatment.

Detailed Description

Primary Objective:

  • To assess in patients with R/R T-ALL or AML
  • Maximum tolerated dose of STI-6129
  • Phase 2 recommended dose
  • Safety of STI-6129

Secondary Objectives:

  • Efficacy of STI-6129, overall response rate (CR+CRi+MLFS)
  • Evaluate rate of negative measurable residual disease (MRD)
  • Evaluate overall survival, duration of response, event-free survival
  • No. of patients transitioning to stem-cell transplantation

Exploratory Objectives:

  • Evaluate the association of biomarkers with safety and efficacy in patients with R/R T-ALL or AML treated with STI-6129 CD38 ADC STI-6129 - R/R T-ALL, AML

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • To be enrolled in the study, patients must satisfy all inclusion criteria, as follows:
  • Age greater than or equal to 18 years.
  • Confirmed diagnosis of R/R T-ALL or R/R AML by bone marrow evaluation. Note that patients must have failed treatment with available therapies known to be active for treatment of their T-ALL/AML
  • ECOG performance status of 0, 1, or 2
  • Pulse oximetry greater than or equal to 92% on room air
  • Be willing and able to comply with the study schedule and all other protocol requirements
  • Females of childbearing potential (FCBP), defined as a sexually mature woman who has not undergone a hysterectomy or tubal ligation or who has not been naturally postmenopausal for at least 24 consecutive months, must have a negative pregnancy test during the Screening Period prior to treatment. All heterosexually active FCBP and all heterosexually active male patients must agree to use effective methods of birth control throughout the study

Exclusion Criteria

  • To be enrolled in the study, patients must not satisfy any of the following exclusion criteria:
  • A diagnosis of other malignancies if the malignancy has required therapy within the last 3 months or is not in complete remission. Exceptions are non-metastatic basal cell or squamous cell carcinomas of the skin or prostate cancer or in situ cancer that does not require further active treatment or is well under control
  • Treatment with an allogeneic hematopoietic stem cell transplantation (HSCT) within 3 months prior to the planned infusion of STI-6129, or active graft-versus-host disease (GVHD) following the allogeneic transplant, or a requirement for currently receiving immunosuppressive therapy following the allogeneic transplant.
  • Must be off calcineurin inhibitors for at least 4 weeks prior to study treatment.
  • New York Heart Association (NYHA) class greater than or equal to 3
  • Left ventricular ejection fraction (LVEF) \< 40%.
  • The following baseline chemistry laboratory results at Screening:
  • Serum creatinine \> 2.0 x the upper limit of normal (ULN), or estimated creatinine clearance \< 60 mL/min (using the Cockcroft-Gault equation).
  • Serum aspartate aminotransferase (AST) or alanine aminotransferase (ALT) \> 3x the upper limit of normal (ULN) or serum total bilirubin \> 1.5x ULN (except for patients in or leukemia involvement)
  • Pregnancy or currently breastfeeding

Arms & Interventions

Part 2 (dose expansion)

Experimental

Participants will receive the dose of STI-6129 found in Part 1 of the study.

Intervention: Part 1 (STI-6129) (Drug)

Part 1 (dose escalation)

Experimental

Participants of the first group will receive the lowest dose level. Participants of each new group will receive a higher dose than the group before it, if no intolerable side effects were seen. This will continue until the highest tolerable dose of STI-6129 is found.

Intervention: Part 1 (STI-6129) (Drug)

Part 1 (dose escalation)

Experimental

Participants of the first group will receive the lowest dose level. Participants of each new group will receive a higher dose than the group before it, if no intolerable side effects were seen. This will continue until the highest tolerable dose of STI-6129 is found.

Intervention: Part 2 (STI-6129) (Drug)

Part 2 (dose expansion)

Experimental

Participants will receive the dose of STI-6129 found in Part 1 of the study.

Intervention: Part 2 (STI-6129) (Drug)

Outcomes

Primary Outcomes

Severity of the adverse events (Aes) -The severity of the adverse events (Aes) will be graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) V.5

Time Frame: through completion of study or an average of 1 year.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

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