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Terminated Phase 1 Interventional

A Study to Assess AMG 701 Montherapy, or in Combination With Pomalidomide, With or Without, Dexamethasone in Subjects With Relapsed or Refractory Multiple Myeloma

ClinicalTrials.gov ID: NCT03287908

Public ClinicalTrials.gov record NCT03287908. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 29, 2026, 10:32 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1/2 Open-label Study Evaluating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of AMG 701 Monotherapy, or in Combination With Pomalidomide, With and Without Dexamethasone in Subjects With Relapsed or Refractory Multiple Myeloma (ParadigMM-1B)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary purpose of the phase 1 part of the study is to evaluate safety and tolerability of AMG 701 monotherapy to identify the RP2D for AMG 701 monotherapy followed by a dose-confirmation part to gather further safety data for AMG 701 monotherapy at the RP2D in adult subjects with relapsed/refractory multiple myeloma (RRMM). In addition, this study will include a sequential dose exploration part to identify the RP2D of AMG 701 in combination with pomalidomide, with and without dexamethasone (AMG 701-P+/-d). Phase 2 will consist of the dose-expansion part to gain further efficacy and safety experience with AMG 701 monotherapy in adult subjects with RRMM.

Study identification

NCT ID
NCT03287908
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
Amgen
Industry
Enrollment
174 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 12, 2017
Primary completion
Jun 29, 2023
Completion
Jun 29, 2023
Last update posted
Oct 7, 2025

2017 – 2023

United States locations

U.S. sites
17
U.S. states
14
U.S. cities
15
Facility City State ZIP Site status
Mayo Clinic - Arizona Scottsdale Arizona 85259 —
University of Arkansas for Medical Sciences Myeloma Institute Slot 816 Little Rock Arkansas 72205 —
Mayo Clinic Florida Jacksonville Florida 32224 —
Winship Cancer Institute Emory U Atlanta Georgia 30322 —
University of Chicago Medical Center - Multiple Myeloma Research Consortium Chicago Illinois 60637 —
Dana Farber Cancer Institute Boston Massachusetts 02215 —
Mayo Clinic Rochester Minnesota 55905 —
Washington University St Louis Missouri 63110 —
Hackensack University Medical Center Hackensack New Jersey 07601 —
Icahn School of Medicine at Mount Sinai Hackensack New Jersey 07601 —
Columbia University Medical Center New York New York 10032 —
New York Presbyterian Hospital, Weill Cornell Medical College New York New York 10065 —
Levine Cancer Institute Charlotte North Carolina 28204 —
Wake Forest Baptist Health Winston-Salem North Carolina 27157 —
University of Texas MD Anderson Cancer Center Houston Texas 77030 —
University of Utah Huntsman Cancer Institute Salt Lake City Utah 84112 —
The Medical College of Wisconsin Milwaukee Wisconsin 53226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03287908, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 7, 2025 · Synced Sep 29, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03287908 live on ClinicalTrials.gov.

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