A Study of BMS-986340 as Monotherapy and as Combination Therapy in Participants With Advanced Solid Tumors

June 2, 2026 updated by: Bristol-Myers Squibb

A Phase 1/2 Study of BMS-986340 as Monotherapy and as Combination Therapy in Participants With Advanced Solid Tumors

The purpose of this study is to assess the safety, tolerability, and recommended dose(s) of BMS-986340 as monotherapy and in combination with nivolumab, docetaxel, or Pumitamig in participants with advanced solid tumors. This study is a first-in-human (FIH) study of BMS-986340 in participants with advanced solid tumors.

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Recruiting

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Interventional

Enrollment (Estimated)

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
1109

Phase

Phase

The stage of a clinical trial studying a drug or biological product, based on definitions developed by the U.S. Food and Drug Administration (FDA). The phase is based on the study's objective, the number of participants, and other characteristics. There are five phases: Early Phase 1 (formerly listed as Phase 0), Phase 1, Phase 2, Phase 3, and Phase 4. Not Applicable is used to describe trials without FDA-defined phases, including trials of devices or behavioral interventions.
  • Phase 2
  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact

The name and contact information for the person who can answer enrollment questions for a clinical study. Each location where the study is being conducted may also have a specific contact, who may be better able to answer those questions.
  • Name: First line of the email MUST contain NCT # and Site #.

Study Contact Backup

  • Name: BMS Clinical Trials Contact Center www.BMSClinicalTrials.com
  • Phone Number: 855-907-3286
  • Email: Clinical.Trials@bms.com

Study Locations

  • Australia
    • New South Wales
      • Blacktown, New South Wales, Australia, 2148
        • Recruiting
        • Blacktown Hospital
        • Contact:
          • Adnan Nagrial, Site 0057
          • Phone Number: +61 02 86705071
      • Liverpool, New South Wales, Australia, 2170
        • Recruiting
        • Liverpool Hospital
        • Contact:
          • Abhijit Pal, Site 0058
          • Phone Number: 61287389744
    • Queensland
      • Brisbane, Queensland, Australia, 4102
        • Recruiting
        • Princess Alexandra Hospital
        • Contact:
          • Aaron Hansen, Site 0054
          • Phone Number: 61731765564
    • Victoria
      • Malvern, Victoria, Australia, 3144
        • Recruiting
        • Cabrini Hospital - Malvern
        • Contact:
          • Shehara Mendis, Site 0053
          • Phone Number: (03)95083434
      • Melbourne, Victoria, Australia, 3065
        • Recruiting
        • St Vincent's Hospital
        • Contact:
          • Melissa Moore, Site 0055
          • Phone Number: 61392313155
    • Western Australia
      • Nedlands, Western Australia, Australia, 6009
        • Recruiting
        • One Clinical Research
        • Contact:
          • Muhammad Khattak, Site 0056
          • Phone Number: +61 08 6279 9466
  • Canada
      • Ottawa, Canada, K1H 8L6
        • Recruiting
        • The Ottawa Hospital Cancer Centre
        • Contact:
          • John Hilton, Site 0016
          • Phone Number: (613)737-7700
    • Alberta
      • Edmonton, Alberta, Canada, T6X 1E8
        • Recruiting
        • Cross Cancer Institute
        • Contact:
          • Quincy Chu, Site 0027
          • Phone Number: 7804328248
    • British Columbia
      • Vancouver, British Columbia, Canada, V5Z 4E6
        • Recruiting
        • BC Cancer Vancouver
        • Contact:
          • Anna Tinker, Site 0030
          • Phone Number: 604-877-6000
    • Ontario
      • Hamilton, Ontario, Canada, L8V5C2
        • Recruiting
        • Hamilton Health Sciences-Juravinski Cancer Centre
        • Contact:
          • Sebastien Hotte, Site 0029
          • Phone Number: 905-387-9495
      • Toronto, Ontario, Canada, M5G 2M9
        • Completed
        • Local Institution - 0009
    • Quebec
      • Montreal, Quebec, Canada, H2X 0A9
        • Recruiting
        • Centre Hospitalier de luniversite de Montreal
        • Contact:
          • Rahima Jamal, Site 0015
          • Phone Number: 51489080008444
  • Germany
      • Dresden, Germany, 01307
        • Recruiting
        • Universitaetsklinikum Carl Gustav Carus Dresden-University Cancer Center Early Clinical Trial Unit
        • Contact:
          • Martin Wermke, Site 0010
          • Phone Number: +493514587566
      • Essen, Germany, 45147
        • Recruiting
        • Universitaetsklinikum Essen
        • Contact:
          • Stefan Kasper-Virchow, Site 0018
          • Phone Number: 00492017233449
      • Frankfurt, Germany, 60590
        • Recruiting
        • Universitätsklinikum Frankfurt
        • Contact:
          • Martin Sebastian, Site 0020
          • Phone Number: +496963016217
      • Würzburg, Germany, 97078
        • Recruiting
        • Universitaetsklinikum Wuerzburg
        • Contact:
          • Cyrus Sayehli, Site 0019
          • Phone Number: 4993120140964
    • Baden-Wurttemberg
      • Ulm, Baden-Wurttemberg, Germany, 89081
        • Completed
        • Local Institution - 0044
  • Israel
    • Central District
      • Petah Tikva, Central District, Israel, 4941492
        • Recruiting
        • Rabin Medical Center
        • Contact:
          • Salomon Stemmer, Site 0036
          • Phone Number: 97239378076
      • Ramat Gan, Central District, Israel, 5265601
        • Recruiting
        • Sheba Medical Center
        • Contact:
          • Tamar Beller, Site 0038
          • Phone Number: 97235302542
      • Ramat Gan, Central District, Israel, 5265601
        • Withdrawn
        • Local Institution - 0035
    • Northern District
      • Haifa, Northern District, Israel, 3109601
        • Recruiting
        • Rambam Health Care Campus
        • Contact:
          • Ruth Perets, Site 0039
          • Phone Number: +972-47776700
    • Tell Abīb
      • Tel Aviv, Tell Abīb, Israel, 6423906
        • Recruiting
        • Sourasky Medical Center
        • Contact:
          • Ravit Geva, Site 0037
          • Phone Number: 97236973082
  • Italy
      • Milan, Italy, 20133
        • Recruiting
        • Fondazione IRCCS Istituto Nazionale dei Tumori-Struttura Complessa Oncologia Medica 1
        • Contact:
          • Filippo De Braud, Site 0024
          • Phone Number: 390223903066
      • Naples, Italy, 80131
        • Recruiting
        • Istituto Nazionale Tumori Irccs Fondazione Pascale
        • Contact:
          • Paolo Ascierto, Site 0034
          • Phone Number: 390815903431
      • Roma, Italy, 00168
        • Recruiting
        • Fondazione Policlinico Universitario Agostino Gemelli IRCCS - Universita Cattolica del Sacro Cuore
        • Contact:
          • Gennaro Daniele, Site 0040
          • Phone Number: +390630153446
      • Siena, Italy, 53100
        • Recruiting
        • ospedale le scotte-U.O.C. Immunoterapia Oncologica
        • Contact:
          • Michele Maio, Site 0025
          • Phone Number: 390577586335
    • Milano
      • Rozzano, Milano, Italy, 20089
        • Recruiting
        • Humanitas
        • Contact:
          • Matteo Simonelli, Site 0023
          • Phone Number: +390282244559
    • Torino
      • Candiolo, Torino, Italy, 10060
        • Recruiting
        • Istituto di Candiolo IRCCS - Fondazione del Piemonte per l'Oncologia
        • Contact:
          • Vanesa Gregorc, Site 0033
          • Phone Number: 390119933250
  • Japan
    • Chiba
      • Kashiwa, Chiba, Japan, 277-8577
        • Recruiting
        • National Cancer Center Hospital East
        • Contact:
          • Yasutoshi Kuboki, Site 0064
          • Phone Number: 81471331111
  • Spain
      • Madrid, Spain, 28040
        • Recruiting
        • Hospital Universitario Fundación Jiménez Díaz-START Madrid-FJD
        • Contact:
          • Victor Moreno Garcia, Site 0013
          • Phone Number: 915504800ext2805
      • Madrid, Spain, 28050
        • Recruiting
        • Centro Integral Oncologico Clara Campal-Hospital HM Universitario Sanchinarro-START Madrid-CIOCC
        • Contact:
          • Emiliano Calvo, Site 0011
          • Phone Number: +34934894304
      • Pamplona, Spain, 31008
        • Recruiting
        • Clinica Universidad de Navarra-oNCOLOGY
        • Contact:
          • Ignacio Melero Bermejo, Site 0012
          • Phone Number: 34948255400
    • Andalusia
      • Málaga, Andalusia, Spain, 29010
        • Recruiting
        • Hospital Universitario Virgen de la Victoria
        • Contact:
          • Javier Garcia Corbacho, Site 0048
          • Phone Number: 951032250
    • Barcelona [Barcelona]
      • Badalona, Barcelona [Barcelona], Spain, 08916
        • Recruiting
        • Institut Catalan d Oncologia (ICO) - Badalona
        • Contact:
          • Cinta Hierro Carbo, Site 0014
          • Phone Number: 34934978925
      • Barcelona, Barcelona [Barcelona], Spain, 08035
        • Recruiting
        • Hospital Universitari Vall d'Hebron
        • Contact:
          • Elena Garralda Cabanas, Site 0049
          • Phone Number: 349327460004910
    • Madrid, Comunidad de
      • Madrid, Madrid, Comunidad de, Spain, 28041
        • Recruiting
        • Hospital Universitario 12 de Octubre
        • Contact:
          • Luis Paz-Ares Rodriguez, Site 0047
          • Phone Number: 0034913908922
  • United States
    • California
      • Clovis, California, United States, 93611
        • Recruiting
        • Community Cancer Institute
        • Contact:
          • Uzair Chaudhary, Site 0032
          • Phone Number: 559-387-1600
      • Los Angeles, California, United States, 90033
        • Recruiting
        • USC/Norris Comprehensive Cancer Center
        • Contact:
          • Anthony El-Khoueiry, Site 0041
          • Phone Number: 323-865-3967
      • Newport Beach, California, United States, 92663
        • Recruiting
        • Hoag Memorial Hospital Presbyterian
        • Contact:
          • Carlos Becerra, Site 0050
          • Phone Number: 949-764-8222
    • Iowa
      • Iowa City, Iowa, United States, 52242
        • Recruiting
        • University of Iowa
        • Contact:
          • Douglas Laux, Site 0062
          • Phone Number: 319-356-1032
    • New Jersey
      • Hackensack, New Jersey, United States, 07601
        • Recruiting
        • John Theurer Cancer Center
        • Contact:
          • Martin Gutierrez, Site 0007
          • Phone Number: 551-996-5863
    • New York
      • New York, New York, United States, 10065
        • Completed
        • Local Institution - 0002
      • New York, New York, United States, 10032
        • Completed
        • Local Institution - 0006
    • Oregon
      • Portland, Oregon, United States, 97213
        • Recruiting
        • Providence Cancer Center Oncology and Hematology Care- Eastside
        • Contact:
          • Rom Leidner, Site 0001
          • Phone Number: 503-215-5696
    • Tennessee
      • Nashville, Tennessee, United States, 37232
        • Recruiting
        • Vanderbilt University Medical Center
        • Contact:
          • Jordan Berlin, Site 0052
          • Phone Number: 615-936-1796
      • Nashville, Tennessee, United States, 37067
        • Not yet recruiting
        • Local Institution - 0063
        • Contact:
          • Site 0063
    • Texas
      • Houston, Texas, United States, 77030
        • Recruiting
        • Houston Methodist Hospital
        • Contact:
          • Maen Abdelrahim, Site 0061
          • Phone Number: 346-241-5495

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria

  • Fresh pre-treatment and on-treatment tumor biopsy must be provided for biomarker analysis.
  • Measurable disease per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 and at least 1 lesion accessible for biopsy. Fine needle biopsy, cytology, and bone lesion biopsies are not acceptable.
  • Eastern Cooperative Oncology Group Performance Status of 0 or 1.
  • Radiographically documented progressive disease on or after the most recent therapy.
  • Received standard-of-care therapies, (except for Part 1C, 2C and 2D, where participants with prior docetaxel use for the advanced/metastatic setting will be excluded), including an available programmed death (ligand)-1 inhibitor known to be effective in the tumor type for which they are being evaluated.
  • Advanced or metastatic disease and have received, be refractory to, not be a candidate for, or be intolerant of existing therapies known to provide clinical benefit for the condition of the participant.

Exclusion Criteria

  • Women who are pregnant or breastfeeding.
  • Primary central nervous system (CNS) malignancy.
  • Untreated CNS metastases.
  • Leptomeningeal metastases.
  • Concurrent malignancy requiring treatment or history of prior malignancy active within 2 years prior to the first dose of study treatment.
  • Active, known, or suspected autoimmune disease.
  • Condition requiring systemic treatment with either corticosteroids within 14 days or other immunosuppressive medications within 30 days of the first dose of study treatment.
  • Prior organ or tissue allograft.
  • Uncontrolled or significant cardiovascular disease.
  • Major surgery within 4 weeks of study drug administration.
  • History of or with active interstitial lung disease or pulmonary fibrosis.
  • Other protocol-defined inclusion/exclusion criteria apply.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Sequential Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm

Participant Group / Arm

A group or subgroup of participants in a clinical trial that receives a specific intervention/treatment, or no intervention, according to the trial's protocol.
Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.
Experimental: Part 1A: BMS-986340 Dose Escalation
Drug: BMS-986340
Specified dose on specified days
Experimental: Part 2A: BMS-986340 Dose Expansion
Drug: BMS-986340
Specified dose on specified days
Experimental: Part 1B: BMS-986340 + Nivolumab Dose Escalation
Drug: BMS-986340
Specified dose on specified days
Drug: BMS-936558-01
Specified dose on specified days
Other Names:
  • Nivolumab
Experimental: Part 2B: BMS-986340 + Nivolumab Dose Expansion
Drug: BMS-986340
Specified dose on specified days
Drug: BMS-936558-01
Specified dose on specified days
Other Names:
  • Nivolumab
Experimental: Part 1C: BMS-986340 + Docetaxel Dose Escalation
Drug: Docetaxel
Specified dose on specified days
Drug: BMS-986340
Specified dose on specified days
Experimental: Part 1A-J: BMS-986340 Dose Escalation
Drug: BMS-986340
Specified dose on specified days
Experimental: Part 1B-J: BMS-986340 + Nivolumab Dose Escalation
Drug: BMS-986340
Specified dose on specified days
Drug: BMS-936558-01
Specified dose on specified days
Other Names:
  • Nivolumab
Experimental: Part 2C: BMS-986340 + Docetaxel Dose Expansion
Drug: Docetaxel
Specified dose on specified days
Drug: BMS-986340
Specified dose on specified days
Experimental: Part 2D: BMS-986340 + Pumitamig Dose Expansion
Drug: BMS-986340
Specified dose on specified days
Drug: Pumitamig
Specified dose on specified days
Other Names:
  • BNT327
  • BMS-986545

What is the study measuring?

Primary Outcome Measures

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
Time Frame
Incidence of adverse events (AEs)
Time Frame: Up to 120 weeks
Up to 120 weeks
Incidence of serious adverse events (SAEs)
Time Frame: Up to 120 weeks
Up to 120 weeks
Incidence of AEs leading to discontinuation
Time Frame: Up to 120 weeks
Up to 120 weeks
Incidence of AEs meeting protocol defined dose-limiting toxicity (DLT) criteria
Time Frame: Up to either 21 or 28 days
Up to either 21 or 28 days
Number of deaths
Time Frame: Up to 120 weeks
Up to 120 weeks

Secondary Outcome Measures

Secondary Outcome Measures

In a clinical study's protocol, a planned outcome measure that is not as important as the primary outcome measure for evaluating the effect of an intervention but is still of interest. Most clinical studies have more than one secondary outcome measure.
Outcome Measure
Time Frame
Pharmacokinetic (PK) parameters of BMS-986340 administered as monotherapy: Maximum concentration (Cmax)
Time Frame: Up to 120 weeks
Up to 120 weeks
PK parameters of BMS-986340 administered as monotherapy: Time to maximum concentration (Tmax)
Time Frame: Up to 120 weeks
Up to 120 weeks
PK parameters of BMS-986340 administered as monotherapy: Area under the concentration-time curve 1 dosing interval (AUC (TAU))
Time Frame: Up to 120 weeks
Up to 120 weeks
PK parameters of BMS-986340 administered as monotherapy: Observed concentration at the end of the dosing interval (Ctau)
Time Frame: Up to 120 weeks
Up to 120 weeks
PK parameters of BMS-986340 administered in combination with nivolumab: Maximum concentration (Cmax)
Time Frame: Up to 120 weeks
Up to 120 weeks
PK parameters of BMS-986340 administered in combination with nivolumab: Time to maximum concentration (Tmax)
Time Frame: Up to 120 weeks
Up to 120 weeks
PK parameters of BMS-986340 administered in combination with nivolumab: Area under the concentration-time curve in 1 dosing interval (AUC(TAU))
Time Frame: Up to 120 weeks
Up to 120 weeks
PK parameters of BMS-986340 administered in combination with nivolumab: Observed concentration at the end of the dosing interval (Ctau)
Time Frame: Up to 120 weeks
Up to 120 weeks
Incidence of anti-drug antibodies to BMS- 986340 when administered as monotherapy
Time Frame: Up to 120 weeks
Up to 120 weeks
Incidence of anti-drug antibodies to BMS- 986340 when administered in combination with nivolumab
Time Frame: Up to 120 weeks
Up to 120 weeks
Objective response rate (ORR) per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 by investigator
Time Frame: At 6 months, 12 months
At 6 months, 12 months
Disease control rate (DCR) per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 by investigator
Time Frame: At 6 months, 12 months
At 6 months, 12 months
Duration of response (DOR) per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 by investigator
Time Frame: At 6 months, 12 months
At 6 months, 12 months
Progression-free survival rate (PFSR) per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 by investigator
Time Frame: At 6 months, 12 months
At 6 months, 12 months
PK parameters of BMS-986340 administered in combination with docetaxel: Cmax
Time Frame: Up to 120 weeks
Up to 120 weeks
PK parameters of BMS-986340 administered in combination with docetaxel: Tmax
Time Frame: Up to 120 weeks
Up to 120 weeks
PK parameters of BMS-986340 administered in combination with docetaxel: AUC(TAU)
Time Frame: Up to 120 weeks
Up to 120 weeks
PK parameters of BMS-986340 administered in combination with docetaxel: Ctau
Time Frame: Up to 120 weeks
Up to 120 weeks
Incidence of anti-drug antibodies to BMS- 986340 when administered in combination with docetaxel
Time Frame: Up to 120 weeks
Up to 120 weeks
PK parameters of BMS-986340 administered in combination with pumitamig: Cmax
Time Frame: Up to 120 weeks
Up to 120 weeks
PK parameters of BMS-986340 administered in combination with pumitamig: Tmax
Time Frame: Up to 120 weeks
Up to 120 weeks
PK parameters of BMS-986340 administered in combination with pumitamig: AUC(TAU)
Time Frame: Up to 120 weeks
Up to 120 weeks
PK parameters of BMS-986340 administered in combination with pumitamig: Ctau
Time Frame: Up to 120 weeks
Up to 120 weeks
Incidence of anti-drug antibodies to BMS-986340 when administered in combination with pumitamig
Time Frame: Up to 120 weeks
Up to 120 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
Bristol-Myers Squibb

Investigators

Investigators

A researcher involved in a clinical study. Related terms include site principal investigator, site sub-investigator, study chair, study director, and study principal investigator.
  • Study Director: Bristol-Myers Squibb, Bristol-Myers Squibb

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
May 27, 2021

Primary Completion (Estimated)

Primary Completion

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure. Whether the clinical study ended according to the protocol or was terminated does not affect this date. For clinical studies with more than one primary outcome measure with different completion dates, this term refers to the date on which data collection is completed for all the primary outcome measures. The "anticipated" primary completion date is the date that the researchers think will be the primary completion date for the study.
August 31, 2031

Study Completion (Estimated)

Study Completion

The date on which the last participant in a clinical study was examined or received an intervention/treatment to collect final data for the primary outcome measures, secondary outcome measures, and adverse events (that is, the last participant's last visit). The "anticipated" study completion date is the date that the researchers think will be the study completion date.
August 31, 2031

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
May 19, 2021

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
May 19, 2021

First Posted (Actual)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
May 20, 2021

Study Record Updates

Last Update Posted (Actual)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
June 4, 2026

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
June 2, 2026

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
June 1, 2026

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • CA052-002
  • U1111-1265-4508 (Other Identifier: WHO)
  • 2023-503651-10 (Other Identifier: EU CTR)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

BMS will provide access to individual anonymized participant data upon request from qualified researchers, and subject to certain criteria. Additional information regarding Bristol Myer Squibb's data sharing policy and process can be found at https://www.bms.com/researchers-and-partners/clinical-trials-and-research.html

IPD Sharing Time Frame

See Plan Description

IPD Sharing Access Criteria

See Plan Description

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • CSR

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

Yes

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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