An Investigational Immunotherapy Study of BMS-986288 Alone and in Combination With Nivolumab in Advanced Solid Cancers

Program Status

Active, not recruiting

Phase

Phase 1

Prior Immunotherapy Allowed

Yes

CRC-directed Trial

No

Drugs

BMS-986288, Nivolumab, Opdivo

Tags

MSI-H/ MMRd, MSS/ MMRp

Comments

Immunotherapy combination: BMS-986288 plus nivolumab (anti PD-1, Opdivo).
BMS-986288 (anti-CTLA-4 probody) is a probody composed of a modified version of ipilimumab (Yervoy), a recombinant human monoclonal antibody directed against the human T-cell receptor cytotoxic T-lymphocyte-associated antigen 4 (anti CTLA-4)
At least one previous line of standard therapy received in the metastatic setting.
Measurable disease. At least one lesion that is biopsiable.

Location Location Status
United States
Local Institution - 0075
Costa Mesa, California 92627
Active, not recruiting
Local Institution - 0050
Orange, California 92868-3201
Active, not recruiting
Local Institution - 0005
Aurora, Colorado 80045
Active, not recruiting
Local Institution - 0002
Baltimore, Maryland 21287
Active, not recruiting
Local Institution - 0004
Saint Louis, Missouri 63110
Active, not recruiting
Local Institution - 0001
Hackensack, New Jersey 07601
Active, not recruiting
Argentina
Local Institution - 0011
Ciudad Autónoma De Buenos Aires, Buenos Aires 1426
Active, not recruiting
Local Institution - 0074
Buenos Aires, Ciudad Autónoma De Buenos Aires C1096AAS
Active, not recruiting
Local Institution - 0014
Córdoba, Cordoba X5000HXL
Active, not recruiting
Local Institution - 0013
Río Cuarto, Cordoba 5800
Active, not recruiting
Local Institution - 0008
ABB, Distrito Federal C1199
Active, not recruiting
Local Institution - 0012
Caba, Distrito Federal C1430
Active, not recruiting
Local Institution - 0017
Buenos Aires 1431
Active, not recruiting
Local Institution - 0016
Buenos Aires C1280AEB
Active, not recruiting
Canada
Local Institution - 0006
Toronto, Ontario M5G 2M9
Active, not recruiting
Local Institution - 0046
Montreal, Quebec H3T 1E2
Active, not recruiting
Local Institution - 0042
Montréal, Quebec H2X 0A9
Active, not recruiting
Chile
Local Institution - 0019
Santiago, Metropolitana 7510032
Active, not recruiting
Local Institution - 0035
Santiago, Metropolitana 7620002
Active, not recruiting
Local Institution - 0009
Santiago, Metropolitana 8420383
Active, not recruiting
Local Institution - 0036
Santiago, Región Metropolitana De Santiago 7500921
Active, not recruiting
Local Institution - 0010
Viña del Mar, Valparaiso 2520598
Active, not recruiting
France
Local Institution - 0034
Bordeaux, Gironde 33075
Active, not recruiting
Local Institution - 0022
Saint-Herblain, Loire-Atlantique 44800
Active, not recruiting
Local Institution - 0018
Bron Cedex 69677
Active, not recruiting
Local Institution - 0026
Marseille 13915
Active, not recruiting
Local Institution - 0015
Paris 75248
Active, not recruiting
Centre Hospitalier intercommunal de Toulon La Seyne sur Mer
Toulon 83100
Active, not recruiting
Italy
Local Institution - 0040
Milan, Lombardia 20133
Active, not recruiting
Local Institution - 0038
Padova, Veneto 35128
Active, not recruiting
Local Institution - 0028
Ancona 60126
Active, not recruiting
Local Institution - 0033
Catanzaro 88100
Active, not recruiting
Local Institution - 0031
Milan 20162
Active, not recruiting
Local Institution - 0039
Roma 00168
Active, not recruiting
Spain
Local Institution - 0056
Barcelona, Barcelona [Barcelona] 08035
Active, not recruiting
Local Institution - 0054
Barcelona, Catalunya [Cataluña] 08036
Active, not recruiting
Local Institution - 0023
Madrid 28041
Active, not recruiting
Local Institution - 0024
Majadahonda 28222
Active, not recruiting
Local Institution - 0055
Sevilla 41013
Active, not recruiting
Local Institution - 0025
València 46026
Active, not recruiting

Inclusion Criteria

Inclusion Criteria:

* Histologic or cytologic confirmation of select solid tumor that is advanced (metastatic, recurrent, and/or unresectable) with measurable disease and have at least 1 lesion accessible for biopsy
* Eastern Cooperative Oncology Group Performance Status of 0 or 1
* Received, and then progressed, relapsed, or been intolerant to, at least 1 standard treatment regimen in the advanced or metastatic setting according to select solid tumor histologies

Exclusion Criteria

Exclusion Criteria:

* Active, known or suspected autoimmune disease
* Active malignancy requiring concurrent intervention
* Primary Central Nervous System (CNS) malignancies or tumors with CNS metastasis as the only site of disease, will be excluded

Other protocol-defined inclusion/exclusion criteria apply

NCT ID

NCT03994601

Date Trial Added

2019-06-21

Updated Date

2024-07-31