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NCT01023880 · ClinicalTrials.gov registry record · Phase 1

Study to Determine the Maximum Tolerated Dose and Evaluate the Efficacy and Safety of CEP-18770 (Delanzomib) in Patients With Relapsed Multiple Myeloma Refractory to the Most Recent Therapy

A Phase 1 study, sponsored by Cephalon.

Terminated
Registry status
Phase 1
Development phase
62
Enrollment target

NCT01023880: Clinical Trial Phase 1 study, sponsored by Cephalon.

NCT01023880 is a Phase 1 study that was terminated before completion, run by Cephalon. The registered enrollment target is 62 participants, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01023880, a Phase 1 study, was terminated before completion, sponsored by Cephalon.

TERMINATED
Registry status
Phase 1
Development phase
62 participants
Enrollment target

Study Summary

The primary objective for part 1 of the study is to determine the maximum tolerated dose (MTD) of CEP-18770 in patients with relapsed and refractory multiple myeloma. The primary objective for part 2 is to evaluate the antitumor activity of CEP-18770 in patients treated at the MTD.

Interventions

  • DRUG CEP-18770

Trial Details

FieldValue
Enrollment Target 62 participants
Start Date 2010-01
Est. Completion 2013-01
Phase Phase 1
Cephalon

64 total trials

Why NCT01023880 stopped before completion

NCT01023880 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 62 participants, a relatively small participant target, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target.

The record links to 0 conditions, and to 1 intervention - of which CEP-18770 is the first listed.

NCT01023880 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01023880 about?

NCT01023880 is a clinical study titled "Study to Determine the Maximum Tolerated Dose and Evaluate the Efficacy and Safety of CEP-18770 (Delanzomib) in Patients With Relapsed Multiple Myeloma Refractory to the Most Recent Therapy". The primary objective for part 1 of the study is to determine the maximum tolerated dose (MTD) of CEP-18770 in patients with relapsed and refractory multiple myeloma. The primary objective for part 2 is to evaluate the antitumor activity of CEP-18770 in patients treated at the MTD.

What is the current status of trial NCT01023880?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 62 participants. The study started on 2010-01. Estimated completion is 2013-01.

What interventions are being tested in trial NCT01023880?

The interventions under investigation include: CEP-18770 (DRUG).

Who is sponsoring clinical trial NCT01023880?

This trial is sponsored by Cephalon, which has 64 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01023880's enrollment target sits among peer trials

62 824th of 2000 higher than 1,173 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01023880, the US trial registry maintained by the National Library of Medicine. NCT01023880 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.