MMRC Horizon One Adaptive Platform Trial Evaluating Therapies in RRMM

Description

This trial is an adaptive platform trial. The structure of the protocol allows the trial to evolve over time. Multiple investigational arms will be included within the trial under a Master Protocol (MP). These investigational arms may be added as appendices at different times depending on whether they are trial-ready and whether accrual in the trial will support another arm. Accrual to an arm will terminate in accord with the arm's appendix to the Master Protocol. The purpose of this proposed structure is to support the recurrent research challenge of efficiently evaluating what is the best therapy for a particular patient.

Conditions

Relapse Multiple Myeloma, Refractory Multiple Myeloma

Study Overview

Study Details

Study overview

This trial is an adaptive platform trial. The structure of the protocol allows the trial to evolve over time. Multiple investigational arms will be included within the trial under a Master Protocol (MP). These investigational arms may be added as appendices at different times depending on whether they are trial-ready and whether accrual in the trial will support another arm. Accrual to an arm will terminate in accord with the arm's appendix to the Master Protocol. The purpose of this proposed structure is to support the recurrent research challenge of efficiently evaluating what is the best therapy for a particular patient.

A Phase II Randomized Adaptive Platform Trial Evaluating Novel Therapies in Relapsed or Refractory Multiple Myeloma

MMRC Horizon One Adaptive Platform Trial Evaluating Therapies in RRMM

Condition
Relapse Multiple Myeloma
Intervention / Treatment

-

Contacts and Locations

Duarte

City of Hope, Duarte, California, United States, 91010

Nashville

Tennessee Oncology, Nashville, Tennessee, United States, 37203

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * For inclusion in the trial, all the following inclusion criteria must be fulfilled, as no waivers will be permitted:
  • * For inclusion in the trial, all the following inclusion criteria must be fulfilled, as no waivers will be permitted:

Ages Eligible for Study

18 Years to 99 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Multiple Myeloma Research Consortium,

Hearn J Cho, MD, PhD, PRINCIPAL_INVESTIGATOR, Multiple Myeloma Research Foundation

Study Record Dates

2030-07-31