CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 33 enrolled
Drug / intervention
LY2787106 +1 moredrug
Likely dose
Not stated in 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/NCT01340976
NCT01340976Phase 1Completed

A Phase 1 Safety Study of LY2787106 in Patients With Cancer and Anemia

Eli Lilly and Company·interventional·Posted Apr 25, 2011·Updated Oct 3, 2018

In Brief

A Phase 1 clinical trial evaluating LY2787106 and Iron Supplementation for Anemia. Completed, enrolled 33 participants across 9 sites.

Detailed Summary

This study will evaluate the safety LY2787106 in participants with cancer and anemia. It will also evaluate when LY2787106 can improve anemia. This study has two parts: Part A is a dose escalation evaluation. Part B is an evaluation of LY2787106 at a defined dose given with and without iron supplementation.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAnemia
CountriesUnited States
Collaborators--

Timeline

Phase 1CompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedApr 25, 2011
Enrollment StartJan 1, 2010
Primary CompletionDec 1, 2014
TodayJul 2, 2026
Enrollment to primary: 4.9 yearsPosted 15.2 years ago

Interventions

LY2787106drug

Administered IV.

Iron Supplementationdietary

Administered orally.