New Adjuvant Trial of Chemotherapy vs Chemo-immunotherapy

PHASE3Active, not recruitingINTERVENTIONAL
Enrollment

210

Participants

Timeline

Start Date

January 13, 2021

Primary Completion Date

April 1, 2030

Study Completion Date

April 1, 2031

Conditions
Non-Small Cell Lung CancerAdjuvant Chemotherapy
Interventions
DRUG

Carboplatin

"Structure: The cis-diamino (cyclobutan-1, 1 dicarboxilate) plating. Stability: 24 hours at ambient temperature in 5% glucose, glucosaline or physiologic saline. It is recommended not to dilute with chlorinated solutions for this could affect the carboplatin.~Route of administration: Intravenous infusion.~Guidelines of Carboplatin administration: According to the standard of each center."

DRUG

Paclitaxel

"Structure: A diterpene whose composition is: 5b, 20-epoxy-1, 2a, 4,7b, 10b, 13a-hexa-hidroxytax-11-en 9 one 4,10-diacetate 2-benzoate 13-ester with (2R,3S)- N-benzoyl-3-phenylisoserine.~Stability: Concentrations of 0.3-1.2 mg/ml in 5% dextrose or normal saline have demonstrated chemical and physical stability for more that 27 hours at ambient temperature (25ºC approximately). The intact vial must be stored between 15º and 25ºC.~Guidelines on Paclitaxel administration: Paclitaxel must be administered by infusion over 3 hours in dextrose (D5W) or normal saline (NS). The concentration must not exceed 1.2 mg/ml."

DRUG

Nivolumab

"Structure: Nivolumab is a soluble protein consisting of 4 polypeptide chains.~Route of administration: Intravenous infusion.~Product Description: Nivolumab (BMS-936558-01) Injection drug product is a sterile, non-pyrogenic, single-use, isotonic aqueous solution formulated in 10 mg/ml.~Storage Conditions: It must be stored at 2 to 8 degrees Cº and protected from light and freezing.~Guidelines: The administration of nivolumab infusion must be completed within 24 hours of preparation.The dose of Nivolumab for the adjuvant treatment is 360 mg administered as an intravenous infusion over 30 minutes every 3 weeks (+/-3 days) for 4 cycles.~For the maintenance adjuvant treatment the dose is nivolumab 480 mg Q4W (+/-3 days) over 30 minutes for 6 months (6 cycles).~Subjects should be carefully monitored during nivolumab administration to follow infusion reactions.~Doses of nivolumab may be interrupted, delayed, or discontinued depending on how well the subject tolerates the treatment."

Trial Locations (30)

10003

Hospital San Pedro De Alcántara, Cáceres

15006

Hospitalario Universitario A Coruña, A Coruña

17007

ICO Girona, Hospital Josep Trueta, Girona

23007

Hospital Universitario de Jaén, Jaén

27003

Hospital Universitario Lucus Augusti, Lugo

28040

Hospital Clínico San Carlos, Madrid

Hospital Universitario Fundación Jiménez Díaz, Madrid

28046

Hospital Universitario la Paz, Madrid

28222

Hospital Puerta de Hierro, Madrid

28922

Hospital Fundación de Alcorcón, Madrid

30120

Hospital Universitario Virgen de la Arrixaca, El Palmar

31008

Complejo Hospitalario de Navarra, Pamplona

35016

Hospital Universitario Insular de Gran canaria, Las Palmas de Gran Canaria

36204

Complexo Hospitalario Universitario De Vigo, Vigo

38009

Hospital Universitario Nuestra Señora La Candelaria, Santa Cruz de Tenerife

41013

Hospital Virgen del Rocío, Seville

46009

Instituto Valenciano De Oncología, Valencia

46010

Hospital Clínico de Valencia, Valencia

46014

Hospital General Universitario de Valencia, Valencia

46026

Hospital Universitario La Fe, Valencia

48013

Hospital de Basurto, Bilbao

48903

Hospital Universitario Cruces, Barakaldo

08916

ICO Badalona, Hospital Germans Trias i Pujol, Badalona

08908

ICO Hospitalet, L'Hospitalet de Llobregat

03010

Hospital General Universitario de Alicante, Alicante

08028

Hospital Universitari Quiron Dexeus, Barcelona

08035

Hospital Universitari Vall d' Hebron, Barcelona

08041

Hospital de la Santa Creu i Sant Pau, Barcelona

08208

Hospital Parc Taulí, Barcelona

07120

Hospital Son Espases, Palma de Mallorca

All Listed Sponsors
lead

Fundación GECP

OTHER