TerminatedPhase 2NCT02161419

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

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.

Checked against the public recordLast updated Jun 25, 2018 · Source: ClinicalTrials.gov

StatusTerminated
PhasePhase 2
U.S. locations32
SponsorBayer
01
Study overview

What this study is about

Purpose
Treatment
Study type
Interventional
Phase
Phase 2
Sponsor
Bayer
Interventions being studied
Drug: Roniciclib (BAY1000394); Drug: Placebo
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

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)

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Study locationBoca Raton, Florida
  • Study locationPort Saint Lucie, Florida
  • Study locationSt Louis, Missouri
  • Study locationHershey, Pennsylvania
  • Study locationPittsburgh, Pennsylvania
  • Study locationCharleston, South Carolina
  • Study locationNashville, Tennessee
  • Study locationBruxelles - Brussel
  • Study locationLiège
  • Study locationBrest
  • Study locationLille
  • Study locationMarseille

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Jun 25, 2018. Always confirm current availability with the study team.

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