Areas of interest (AOI) & competitive research grants

We are currently accepting concepts for the following therapeutic areas. BMS periodically opens RFP Cycles across different therapeutic areas and the pre-concept submission periods will be posted below when available. We strongly encourage all applicants to begin the online application process early to allow adequate time for completion. For a submission to qualify for review, all information including any required uploads must be submitted through the application form prior to the specified end dates for the RFP Cycle.

Therapeutic Area and / or Compound AOIs Posted on BMS.com Pre-Concept Submission Period
Start Date End date
CV-Mavacamten -2024 RFP Cycle 2 Jul 15, 2024 Sept 02, 2024 Sept 13, 2024
Immunology – Sotyktu (Deucravacitinib) – Dermatology Aug 26, 2024 Sept 23, 2024 Nov 14, 2024
Immunology – Sotyktu (Deucravacitinib) - Rheumatology Aug 26, 2024 Sept 23, 2024 Nov 26, 2024


CV-Mavacamten - 2024 RFP Cycle 2


Nonobstructive HCM disease progression and management​


In Scope:

  • Patient journey to diagnosis​
  • Symptom burden​
  • Practice patterns​

Out of Scope:

  • Off-label use of Camzyos
  • Viz-AI algorithm

CAMZYOS impact on cardiac structure and function

In Scope:

  • Association between indicators of remodeling and clinical outcomes.
  • Impact on patients with earlier disease (less symptomatic, milder phenotype)

Out of Scope:

  • Off-label (asymptomatic obstructive HCM; non-obstructive HCM, etc.); head-to-head comparisons between CAMZYOS and other treatments; pre-clinical studies, CYP2C19 genotyping; re-analysis of clinical trial data. Myosin genotyping; re-analysis of clinical trial data​
  • Pediatric populations​
  • Viz-AI algorithm​
  • Repeat of BMS-led studies (Mava-LTE, sub-analysis of clinical data, CMR study)

CAMZYOS echo monitoring.

In Scope:

  • Assess the benefits of innovative technologies to improve quality outcomes and enhance coordination of care, and health equity in patients on CAMZYOS

Out of Scope:

  • Off-label (asymptomatic obstructive HCM; non-obstructive HCM, etc.); head-to-head comparisons between CAMZYOS and other treatments; pre-clinical studies, CYP2C19 genotyping; re-analysis of clinical trial data. Myosin genotyping; re-analysis of clinical trial data​
  • Pediatric populations​
  • Viz-AI algorithm​

Implementation of best practices

In Scope:

  • Decision-making support to include patient-preference
  • Approaches to Workflow optimization and co-management (quality-improvement studies)
  • Approaches that incorporate technology to streamline HCM patient management

Out of Scope:

  • Off-label (asymptomatic obstructive HCM; non-obstructive HCM, etc.); head-to-head comparisons between CAMZYOS and other treatments; pre-clinical studies, CYP2C19 genotyping; re-analysis of clinical trial data. Myosin genotyping; re-analysis of clinical trial data.
  • No Biomarker data
  • Pediatric populations
  • Viz-AI algorithm
  • Non-research-focused concepts

Please note that during an open RFP submission window, clicking on a link to submit your research idea will take you to the FastTrack Investigator Portal and you will receive a message that you are leaving BMS.com. This is part of the normal process.

  • If you are a potential investigator who is interested in seeking support to conduct independent research involving  Nivolumab  in Japan, Taiwan, or Korea, click here
  • If you are a potential investigator who is interested in seeking support for independent research using Apixaban, click here.
  • If you are a potential investigator who is interested in seeking support for non-clinical research using a BMS product, click here
  • If you are a potential investigator who is interested in seeking support for independent research using one of our early pipeline assets, click here

Please click on the product name to see the Full U.S. Prescribing Information for ELIQUIS®, EMPLICITI, NULOJIX®, OPDIVO®, ORENCIA®, SPRYCEL®, YERVOY®, including Boxed WARNINGS for ELIQUIS®, NULOJIX®, and Boxed WARNING for YERVOY® regarding immune-mediated adverse reactions.

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