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Clinical Trials/NCT04445701
NCT04445701
Completed
Phase 1

A Phase 1/2, Dose Escalation Safety and Tolerability Study of AO-176 as Monotherapy and in Combination With Bortezomib and Dexamethasone in Adults With Relapsed or Refractory Multiple Myeloma

Arch Oncology4 sites in 1 country10 target enrollmentNovember 30, 2020

Overview

Phase
Phase 1
Intervention
AO-176
Conditions
Multiple Myeloma
Sponsor
Arch Oncology
Enrollment
10
Locations
4
Primary Endpoint
Phase 1: MTD / RP2D of AO-176 assessed by incidence of dose-limiting toxicities and incidence of treatment-related adverse events (TEAEs) as assessed by CTCAE v5.0
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Open-label, dose escalation study to evaluate the safety, tolerability, pharmacokinetics (PK)/pharmacodynamics and initial efficacy of AO-176 as monotherapy and in combination with dexamethasone and bortezomib in adults with relapsed/refractory multiple myeloma (MM).

Detailed Description

An open-label, multicenter, dose escalation study to evaluate the safety, tolerability and PK/pharmacodynamics of AO-176 in adults with relapsed/refractory multiple myeloma whose disease has progressed following at least 3 prior systemic lines of treatment and must have progressed on the final line of therapy received before being considered for this study. The study will be conducted in 2 phases; Phase 1 is an ascending-dose study of AO-176 monotherapy utilizing the classic 3+3 design, with enrollment of 3 patients per cohort and expansion of the cohort in the event of a dose-limiting toxicity (DLT). Following the dose escalation portion and determination of the monotherapy recommended phase 2 dose (RP2D), an ascending dose escalation study of AO-176 and dexamethasone combined with bortezomib will be evaluated utilizing the same 3+3 dose escalation design. Phase 2 will evaluate the clinical activity of AO-176 plus dexamethasone and bortezomib at the RP2D as determined in Phase 1 Part 2.

Registry
clinicaltrials.gov
Start Date
November 30, 2020
End Date
November 14, 2022
Last Updated
2 years ago
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Sponsor
Arch Oncology
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Confirmed diagnosis of symptomatic MM per IMWG criteria
  • Measurable disease
  • Relapsed or refractory to at least 3 prior systemic lines of therapy for MM
  • Eastern Cooperative Oncology Group (ECOG) status 0-2
  • Resolution of prior therapy-related adverse events
  • Minimum of 2 weeks since last dose of cancer therapy or radiotherapy

Exclusion Criteria

  • Previous Grade 3-4 infusion or hypersensitivity reaction
  • Severe asthma or chronic obstructive pulmonary disease exacerbations requiring hospital admission or steroids
  • Prior treatment with a checkpoint inhibitor (anti-PD-1, PD-L1 or CTLA-4) within 4 weeks.
  • Prior treatment with a therapeutic agent that targets the CD47 axis.

Arms & Interventions

AO-176 Dose Escalation Monotherapy

The dose escalation monotherapy cohorts will initially recruit 3 patients to receive AO-176 in a standard 3+3 design; cohorts will be expanded in the event of a DLT.

Intervention: AO-176

AO-176 + DEX Expansion Cohort

Once the monotherapy RP2D has been established, an expansion cohort of AO-176 + dexamethasone will be enrolled.

Intervention: AO-176 + Dex

AO-176 + DEX + BORT Dose Escalation

Following evaluation of AO-176 + dexamethasone, dose escalation cohorts of AO-176 + dexamethasone + bortezomib will be enrolled. Each dose escalation cohort will initially recruit 3 patients in a standard 3+3 design; cohorts will be expanded in the event of a DLT. The Phase 2 portion of the study will further evaluate the RP2D of AO-176 + DEX + BORT.

Intervention: AO-176 + Dex + Bort

Outcomes

Primary Outcomes

Phase 1: MTD / RP2D of AO-176 assessed by incidence of dose-limiting toxicities and incidence of treatment-related adverse events (TEAEs) as assessed by CTCAE v5.0

Time Frame: 12 months

Safety and tolerability of AO-176 when administered as monotherapy and in combination with dexamethasone or with dexamethasone plus bortezomib in adult patients with R/R MM as assessed by incidence of DLTs and TEAEs as assessed by CTCAE v5.0

Phase 2: Objective response rate (ORR) of AO-176 + DEX + BORT

Time Frame: 12 months

Evaluate the clinical activity of AO-176 + dexamethasone + bortezomib based on ORR using International Myeloma Working Group (IMWG) uniform response criteria

Secondary Outcomes

  • Phase 2: DCR of AO-176 + DEX + BORT(12 months)
  • Phase 1: ORR of single agent AO-176(12 months)
  • Phase 1: Disease control rate (DCR) of single agent AO-176(12 months)
  • Phase 1: Progression-free survival (PFS) of single agent AO-176(12 months)
  • Phase 1: Overall survival (OS) of single agent AO-176(12 months)
  • Phase 2: PFS of AO-176 + DEX + BORT(12 months)
  • Phase 2: OS of AO-176 + DEX + BORT(12 months)
  • Phase 1: Duration of response (DOR) of single agent AO-176(12 months)
  • Phase 2: DOR of AO-176 + DEX + BORT(12 months)

Study Sites (4)

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