08 abril 2016

PM01183 a Fase III Pulmón . FDA Autoriza su Inició con Fecha Junio 2016 .

View of NCT02566993 on 2016_04_04

ClinicalTrials Identifier:NCT02566993
Updated:2016_04_04

Descriptive Information

Brief titleClinical Trial of Lurbinectedin (PM01183)/Doxorubicin (DOX) Versus Cyclophosphamide (CTX), Doxorubicin (DOX) and Vincristine (VCR) (CAV) or Topotecan as Treatment in Patients With Small-Cell Lung Cancer
Official titlePhase III Randomized Clinical Trial of Lurbinectedin (PM01183)/Doxorubicin (DOX) Versus Cyclophosphamide (CTX), Doxorubicin (DOX) and Vincristine (VCR) (CAV) or Topotecan as Treatment in Patients With Small-Cell Lung Cancer (SCLC) Who Failed One Prior Platinum-containing Line (ATLANTIS Trial)
Brief summary
Phase III randomized clinical trial of lurbinectedin (PM01183)/doxorubicin (DOX) versus cyclophosphamide (CTX), doxorubicin (DOX) and vincristine (VCR) (CAV) or topotecan as treatment in patients with small-cell lung cancer (SCLC) who failed one prior platinum-containing line to determine a difference in progression-free survival (PFS) by an Independent Review Committee (IRC) between lurbinectedin (PM01183)/doxorubicin (DOX) and the control arm (CAV) or topotecan and to analyze the median overall survival (OS) and mid- and long-term overall survival (OS at 12, 18 and 24 months).
Detailed description
PhasePhase 3
Study typeInterventional
Study designTreatment
Study designRandomized

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Administrative Data

Organization namePharmaMar
Organization study IDPM1183-C-003-14
SponsorPharmaMar
Health AuthorityUnited States: Food and Drug Administration

Recruitment 

Information :

Status :Not yet recruiting


Start date :2016-06


Primary completion date :


2019-06 (Anticipated)


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