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Terminated Phase 1 Interventional

Phase Ib/II Study of M3814 With Etoposide and Cisplatin in Small Cell Lung Cancer (SCLC) Extensive Disease (ED)

ClinicalTrials.gov ID: NCT03116971

Public ClinicalTrials.gov record NCT03116971. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 2:59 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter Study With an Open Label Phase Ib Part Followed by a Randomized, Placebo-controlled, Double-blind, Phase II Part to Evaluate Efficacy, Safety, Tolerability, and PK of M3814 in Combination With Etoposide and Cisplatin in Subjects With Treatment-naïve Small Cell Lung Cancer (SCLC) Extensive Disease (ED)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

M3814 is an investigational drug under evaluation for treatment of lung cancer. The purpose of the study was to assess the Safety and Efficacy of M3814 in combination with chemotherapy with SCLC ED.

Study identification

NCT ID
NCT03116971
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Enrollment
2 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 24, 2017
Primary completion
Feb 28, 2018
Completion
Feb 28, 2018
Last update posted
Sep 15, 2020

2017 – 2018

United States locations

U.S. sites
16
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
Research site Mesa Arizona 85206
Research site 1 Santa Rosa California 95403
Research site Santa Rosa California 95403
Research site Whittier California 90603
Research site Danbury Connecticut 06810
Research site Norwalk Connecticut 06850
Research site Columbus Georgia 31904
Research site Newnan Georgia 30265
Research site Topeka Kansas 66606
Research site Ashland Kentucky 41101
Research site Billings Montana 59101
Research site Pinehurst North Carolina 28374
Research site Cincinnati Ohio 45229
Research site Portland Oregon 97213
Research site Philadelphia Pennsylvania 19124
Research site Houston Texas 77030

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 64 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03116971, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 15, 2020 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03116971 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →