CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 226 enrolled
Drug / intervention
CC-223drug
Likely dose
CC-223 7.5mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01177397
NCT01177397Phase 2Completed

A Phase 1/2, Multi-Center, Open-Label, Dose Finding Study to Assess the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of the mTOR Kinase Inhibitor CC-223 Administered Orally to Subjects With Advanced Solid Tumors, Non-Hodgkin Lymphoma, or Multiple Myeloma

Celgene·interventional·Posted Aug 9, 2010·Updated Dec 13, 2022

In Brief

A Phase 2 clinical trial evaluating CC-223 for Multiple Myeloma and 6 related conditions. Completed, enrolled 226 participants across 16 sites in 4 countries.

Detailed Summary

The main purpose of this first human study with CC-223 is to assess the safety and action of a new class of experimental drug (dual mTOR inhibitors) in patients with advanced tumors unresponsive to standard therapies and to determine the appropriate dose and tumor type for later-stage clinical trials.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesFrance, Spain, United Kingdom, United States
Collaborators--

Timeline

Phase 2CompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
First PostedAug 9, 2010
Enrollment StartJul 20, 2010
Primary CompletionNov 15, 2016
Study CompletionDec 9, 2016
TodayJul 2, 2026
Enrollment to primary: 6.3 yearsPosted 15.9 years ago

Interventions

CC-223drug

Part A: (closed to enrollment) Dose level starts with 7.5mg daily taken by mouth in cycles of 28 days. Level increases for different patient cohorts in 100% or 50% increments until optimal dose level is established for further study. Treatment continues for as long as patient benefits (i.e., until disease progression or unacceptable toxicity). Part B: (closed to enrollment) Optimal dose is administered in 28 day cycles until disease progression.