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NCT02720510 · MORE INFO

Limitations, agreements, and source contact

A Trial Evaluating Efficacy & Safety of RVD +/- Panobinostat in Transplant Eligible, Newly Diagnosed Multiple Myeloma (NDMM) · Source last updated 2018-07-24

Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.

certain Agreement
other Details
The terms and conditions of Novartis' agreements with its investigators may vary. However, Novartis does not prohibit any investigator from publishing. Any publications from a single-site are postponed until the publication of the pooled data (ie, data from all sites) in the clinical trial.
pi Sponsor Employee
false
restriction Type
OTHER
restrictive Agreement
true
limitations And Caveats
description
This study was terminated prematurely. The reason for study termination was not related to challenges linked to efficacy or safety data but instead, had faced unanticipated challenges with enrollment.
point Of Contact
email
Novartis.email@novartis.com
organization
Novartis Pharmaceuticals
phone
862-778-8300
title
Study Director
Complete source fields
certain Agreement
other Details
The terms and conditions of Novartis' agreements with its investigators may vary. However, Novartis does not prohibit any investigator from publishing. Any publications from a single-site are postponed until the publication of the pooled data (ie, data from all sites) in the clinical trial.
pi Sponsor Employee
false
restriction Type
OTHER
restrictive Agreement
true
limitations And Caveats
description
This study was terminated prematurely. The reason for study termination was not related to challenges linked to efficacy or safety data but instead, had faced unanticipated challenges with enrollment.
point Of Contact
email
Novartis.email@novartis.com
organization
Novartis Pharmaceuticals
phone
862-778-8300
title
Study Director

Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f

Preserved source evidence · Not medical advice