Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01222286 · ClinicalTrials.gov registry record · Phase 2

Study on the Anti-tumor Activity, Safety and Pharmacology of IPH2101 in Patients With Smoldering Multiple Myeloma

A Phase 2 study of Smoldering Multiple Myeloma, sponsored by Innate Pharma.

Completed
Registry status
Phase 2
Development phase
30
Enrollment target
5
Study locations

NCT01222286 is a Phase 2 study of Smoldering Multiple Myeloma that has completed, run by Innate Pharma. The registered enrollment target is 30 participants, below the 798-participant average among 20 other Smoldering Multiple Myeloma trials with a reported enrollment target (96% lower). The trial reports 5 study locations across 5 states.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01222286, a Phase 2 study of Smoldering Multiple Myeloma, has completed, sponsored by Innate Pharma.

COMPLETED
Registry status
Phase 2
Development phase
30 participants
Enrollment target
5
Study locations

Study Summary

The purpose of this study is to evaluate the anti-tumor activity, safety and pharmacology of two dose regimens (0.2 and 2 mg/kg)of IPH2101 in patients with Smoldering Multiple Myeloma.

Interventions

  • DRUG IPH2101

Study Locations (5)

Massachusetts

  • Dana-Farber Cancer Institute - Boston

New York

  • Mount Sinai School of Medicine - New York

Ohio

  • Ohio State University - Columbus

Pennsylvania

  • Hospital of the University of Pennsylvania - Philadelphia

Tennessee

  • Sarah Cannon Research Institute - Nashville

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2010-09
Est. Completion 2013-01
Phase Phase 2

Sponsor

Innate Pharma

12 total trials

What the Registry Record Tells You About NCT01222286

The ClinicalTrials.gov registry entry for NCT01222286 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 798-participant average among 20 other Smoldering Multiple Myeloma trials with a reported enrollment target (96% lower). The listed sponsor is Innate Pharma, which has 12 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Smoldering Multiple Myeloma appearing as the primary indexed condition, and to 1 intervention - of which IPH2101 is the first listed.

NCT01222286 reports 5 study locations spanning 5 distinct geographic areas - top geographies include Massachusetts, New York, Ohio.

Frequently Asked Questions

What is clinical trial NCT01222286 about?

NCT01222286 is a clinical study titled "Study on the Anti-tumor Activity, Safety and Pharmacology of IPH2101 in Patients With Smoldering Multiple Myeloma". The purpose of this study is to evaluate the anti-tumor activity, safety and pharmacology of two dose regimens (0.2 and 2 mg/kg)of IPH2101 in patients with Smoldering Multiple Myeloma.

What is the current status of trial NCT01222286?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 30 participants. The study started on 2010-09. Estimated completion is 2013-01.

What conditions does trial NCT01222286 study?

This clinical trial studies the following conditions: Smoldering Multiple Myeloma.

What interventions are being tested in trial NCT01222286?

The interventions under investigation include: IPH2101 (DRUG).

Who is sponsoring clinical trial NCT01222286?

This trial is sponsored by Innate Pharma, which has 12 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01222286 being conducted?

This trial has 5 study locations across Massachusetts, New York, Ohio, Pennsylvania, Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Smoldering Multiple Myeloma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.