Study of BMS-986012 in Subjects With Small Cell Lung Caner

NCT02949895 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 7

Last updated 2019-08-12

No results posted yet for this study

Summary

A study to evaluate safety and tolerability of BMS-986012 in patients with small cell lung cancer

Conditions

Interventions

DRUG

BMS-986012

DRUG

Cisplatin

DRUG

Etoposide

Sponsors & Collaborators

Principal Investigators

  • Bristol-Myers Squibb · Bristol-Myers Squibb

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-11-29
Primary Completion
2017-08-29
Completion
2017-08-29

Countries

  • Japan

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02949895 on ClinicalTrials.gov