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Completed Phase 2 Interventional Results available

A Study of Melphalan Flufenamide (Melflufen) Plus Dexamethasone in Patients With Relapsed or Refractory Multiple Myeloma

ClinicalTrials.gov ID: NCT02963493

Public ClinicalTrials.gov record NCT02963493. 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 Oct 18, 2026, 7:40 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 Single Arm, Open-Label, Phase 2 Study of Melflufen in Combination With Dexamethasone in Patients With Relapsed Refractory Multiple Myeloma Who Are Refractory to Pomalidomide and/or an Anti-CD38 Monoclonal Antibody

Brief summary

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

This study will evaluate melflufen in combination with dexamethasone in adult patients with relapsed or refractory multiple myeloma in whose disease is refractory to pomalidomide and/or an anti-CD38 monoclonal antibody. All patients in the study will be treated with melflufen on Day 1 and dexamethasone on Days 1, 8, 15 and 22 of each 28-day cycle.

Study identification

NCT ID
NCT02963493
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Oncopeptides AB
Industry
Enrollment
157 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
Dec 28, 2016 (Actual)
Primary completion
Oct 22, 2020 (Actual)
Completion
Nov 16, 2021 (Actual)
Last update posted
Nov 22, 2022

2016 – 2021

United States locations

U.S. sites
9
U.S. states
8
U.S. cities
9
Facility City State ZIP Site status
Innovative Clinical Research Institute (ICRI) Whittier California 90603 —
University of Florida Gainesville Florida 32610 —
RUSH Chicago Illinois 60612 —
Dana Farber Cancer Institute Boston Massachusetts 02215 —
Karmanos Cancer Center Detroit Michigan 48201 —
Memorial Sloan Kettering Cancer Center New York New York 10065 —
Hudson Valley Hematology Oncology Poughkeepsie New York 10532 —
UPMC Hillman Cancer Insitute Pittsburgh Pennsylvania 15232 —
Baylor Dallas Texas 75246 —

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 11 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02963493, 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 Nov 22, 2022 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02963493 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →