Lung Cancer Clinical Trial

RONICICLIB / Placebo in Combination With Chemotherapy in Small Cell Lung Cancer

Summary

This is a study to investigate the potential clinical benefit of roniciclib when given in combination with chemotherapy Carboplatin / Etoposide or Cisplatin / Etoposide as first line treatment in patients with extensive disease small cell lung cancer. Approximately 140 patients will be randomized (1:1) to receive treatment with either roniciclib or placebo in combination with chemotherapy.

Roniciclib is an oral (i.e. taken by mouth) protein kinase inhibitor. A kinase inhibitor targets certain key proteins that are essential for the survival of the cancer cell. The growth of the tumor may be decreased by preventing these specific proteins from functioning. By specifically targeting these proteins, roniciclib in combination with chemotherapy may stop cancer growth.

The primary endpoint (the most meaningful result to be tracked) of this study is based on the progression free survival, i.e. the time the disease is not worsening. The aim is to show that the therapy with roniciclib in combination with chemotherapy prolongs the time the disease is not worsening in this patient population compared to patients receiving placebo in combination with chemotherapy.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Male or female subjects aged ≥18 years (or country-specific legal age of maturity, if >18 years)
Histologically or cytologically confirmed (extensive-stage disease) ED SCLC (small cell lung cancer)
At least 1 solid tumor lesion measurable by computer tomography (CT) scan or magnetic resonance imaging (MRI) according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1
Eastern Cooperative Oncology Group (ECOG) performance status of 0 - 1

Exclusion Criteria:

Prior systemic anticancer therapy for SCLC (including previous therapy with a cyclin-dependent kinase [CDK] inhibitor)

Study is for people with:

Lung Cancer

Phase:

Phase 2

Estimated Enrollment:

142

Study ID:

NCT02161419

Recruitment Status:

Terminated

Sponsor:

Bayer

Check Your Eligibility

Let’s see if you might be eligible for this study.

What is your age and gender ?

Submit

There are 32 Locations for this study

See Locations Near You


Boca Raton Florida, 33486, United States

Port Saint Lucie Florida, 34952, United States

Saint Louis Missouri, 63110, United States

Hershey Pennsylvania, 17033, United States

Pittsburgh Pennsylvania, 15232, United States

Charleston South Carolina, 29425, United States

Nashville Tennessee, 37232, United States

Bruxelles - Brussel , 1200, Belgium

Liege , 4000, Belgium

Brest , 29285, France

Lille Cedex , 59020, France

Marseille Cedex 20 , 13915, France

Paris , 75020, France

Heidelberg Baden-Württemberg, 69126, Germany

Oldenburg Niedersachsen, 26121, Germany

Essen Nordrhein-Westfalen, 45147, Germany

Grosshansdorf , 22927, Germany

Budapest , 1121, Hungary

Matrahaza , 3233, Hungary

Torokbalint , 2045, Hungary

Genova Liguria, 16132, Italy

Monza-Brianza Lombardia, 20900, Italy

Sondrio Lombardia, 23035, Italy

Torino Piemonte, 10043, Italy

Kurume Fukuoka, 830-0, Japan

Bunkyo Tokyo, 113-8, Japan

Seongnam-si Gyeonggido, 463-7, Korea, Republic of

Seoul , 05505, Korea, Republic of

Seoul , 120-7, Korea, Republic of

Gdansk , 80-95, Poland

Szczecin-Zdunowo , 70-89, Poland

Warszawa , 02-78, Poland

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Phase:

Phase 2

Estimated Enrollment:

142

Study ID:

NCT02161419

Recruitment Status:

Terminated

Sponsor:


Bayer

How clear is this clinincal trial information?

×

Introducing, the Journey Bar

Use this bar to access information about the steps in your cancer journey.

Please confirm you are a US based health care provider:

Yes, I am a health care Provider No, I am not a health care provider