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Clinical Trials/NCT03763318
NCT03763318
Completed
Phase 1

A Phase 1b/2 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Clinical Activity of EQ001 in Subjects With Newly Diagnosed Acute Graft Versus Host Disease

Equillium16 sites in 1 country30 target enrollmentJuly 15, 2019

Overview

Phase
Phase 1
Intervention
EQ001
Conditions
Acute-graft-versus-host Disease
Sponsor
Equillium
Enrollment
30
Locations
16
Primary Endpoint
Number of Treatment Emergent Adverse Events
Status
Completed
Last Updated
last year

Overview

Brief Summary

This is a multi-center study to evaluate the safety, tolerability, PK, PD, and clinical activity of EQ001 in subjects with Acute Graft Versus Host Disease (aGVHD).

Detailed Description

The study will enroll approximately 100 subjects in two (2) parts: Part A is an open label study and will enroll approximately 40 evaluable subjects with aGVHD across 4 cohorts. The total number of patients will depend on the number of dose escalations necessary to enable a decision to be made on the recommended dose to take forward into Part B of the study. The planned dose escalation will start with cohort 1, where subjects will receive EQ001 administered intravenously every two weeks for a total of 5 doses. Part B is a randomized, double-blind, placebo-controlled study and will enroll approximately 60 additional subjects, randomized in a 2:1 ratio to either active treatment EQ001 (40) or placebo (20). Subjects will receive either EQ001 or placebo administered intravenously every two weeks for a total of 5 doses.

Registry
clinicaltrials.gov
Start Date
July 15, 2019
End Date
November 21, 2022
Last Updated
last year
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Sponsor
Equillium
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Male or female subject at least 18 years of age for Part A, and at least 12 years of age for Part B.
  • Recipients of allogeneic hematopoietic stem cell transplantation (alloHSCT) using myeloablative or non myeloablative conditioning regimens.
  • Have a clinical diagnosis of acute GVHD requiring systemic immune suppressive therapy.
  • Deemed by the investigator to be likely to comply with the planned procedure as required by the protocol for the duration of the study

Exclusion Criteria

  • Presence of morphologic relapsed primary malignancy, treatment for relapse after alloHSCT was performed, or requirement for rapid immunosuppressive treatment withdrawal for early malignancy relapse.
  • Evidence of graft failure based on cytopenia(s), and as determined by the investigator.
  • Evidence of post-transplant lymphoproliferative disease.
  • Any prior therapy for acute GVHD, except for alloHSCT prophylaxis regimens or systemically administered corticosteroids.
  • As determined by the investigator, any medical, psychiatric, or other condition or circumstance that is likely to negatively affect: the subject's participation in this clinical study, the subject's safety, or the reliability of the study data.

Arms & Interventions

EQ001 Dose Escalation (Part A)

Open label EQ001 administered by intravenous infusion every two weeks for a total of 5 doses.

Intervention: EQ001

EQ001 (Part B)

EQ001 administered in a blinded fashion using the optimal dose selected from Part A by intravenous infusion every two weeks for a total of 5 doses.

Intervention: EQ001

EQ001 Placebo (Part B)

Placebo administered in a blinded fashion by intravenous infusion every two weeks for a total of 5 doses.

Intervention: EQ001 Placebo

Outcomes

Primary Outcomes

Number of Treatment Emergent Adverse Events

Time Frame: Study Day 85

Number of participants with treatment-related adverse events as assessed by the Common Terminology Criteria for Adverse Events (CTCAE) v5.0.

Overall Response Rate

Time Frame: Study Day 29

Overall Response Rate (ORR) is defined as the number of subjects with a partial response (PR), very good partial response (VGPR), or complete response (CR) who are alive at Day 29. Subjects must not have received new systemic therapy for aGVHD before the Day 29 Visit.

Secondary Outcomes

  • Time to Maximum EQ001serum Concentration, Tmax(Day 337)
  • Maximum EQ001 Serum Drug Concentration, Cmax(Study Day 337)
  • Minimum EQ001 Serum Drug Concentration, Cmin(Study Day 337)
  • Total EQ001 Exposure Across Time, AUC (From Zero to Infinity)(Study Day 337)
  • Half Life of EQ001, t1/2(Study Day 337)
  • Volume of Distribution of EQ001, Vd(Study Day 337)
  • Clearance, Cl(Study Day 337)
  • Inflammatory Markers(Study Day 337)
  • CD6 Receptor Expression Levels(Study Day 85)

Study Sites (16)

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