The treatment landscape for multiple myeloma (MM) has advanced substantially, moving from conventional chemotherapy to increasingly sophisticated combinations that include proteasome inhibitors, immunomodulatory agents, anti-CD38 monoclonal antibodies, CAR T-cell therapies, and bispecific antibodies. Although these advances have improved survival and broadened treatment options across the disease continuum, relapse remains, and refractory disease, treatment resistance, cumulative toxicity, and access barriers continue to constrain durable disease control. As care becomes more individualized and sequencing decisions more complex, there remains a clear need for novel treatment strategies that can deepen responses, overcome resistance mechanisms, and extend meaningful benefit to patients with heavily pretreated or high-risk disease. Within this context, emerging trispecific antibodies (TsAbs) may represent a next-generation immunotherapeutic approach designed to simultaneously engage multiple tumor antigens and immune effector pathways, with the potential to enhance efficacy while addressing key limitations of existing T-cell–redirecting therapies.
Early clinical data suggests that trispecific antibody approaches may offer meaningful clinical activity in heavily pretreated relapsed/refractory MM, with investigational agents designed to target both BCMA and GPRC5D while engaging CD3-positive T cells. Although these findings remain early and require continued evaluation, they underscore the scientific rationale for BCMA and GPRC5D dual-antigen targeting as a strategy to address tumor heterogeneity, antigen escape, and acquired resistance (van de Donk et al., ASCO 2025 Abstract 7505; Popat et al., EHA 2025 Abstract S100).
At the same time, the rapid pace of innovation is widening educational gaps for hematology/oncology HCPs who must interpret emerging data, anticipate evolving practice implications, and translate novel mechanisms into patient-centered decision-making.
J&J is looking to support independent medical education that will help prepare clinicians to recognize limitations of current MM care, and evaluate emerging trispecific data critically, recognize the unique MOA and scientific rationale for BCMA and GPRC5D dual-antigen targeting, understand where these agents fit in the evolving MM paradigm, create awareness of new and enrolling clinical trials with TsAbs, and support safe, evidence-informed adoption if and when these therapies enter clinical practice.
EDUCATIONAL NEED J&J has determined, through literature searches, insights, and outcomes the following areas of educational needs of healthcare providers:
• Understanding the scientific rationale and mechanistic differentiation of trispecific antibodies in MM, including how BCMA and GPRC5D dual-antigen targeting may overcome disease heterogeneity and resistance mechanisms, enabling greater depth and durability of response relative to existing therapeutic approaches
• Interpreting early-phase efficacy and safety data with appropriate clinical context, including response depth (including MRD), durability, patient population, and limitations of immature evidence.
• Assessing potential implications for treatment sequencing, patient selection, toxicity monitoring, and integration into multidisciplinary care pathways as the evidence base matures.
EXPECTED OUTCOMES AND MEASUREMENT Grant applicants must be willing to adhere to our impact reporting timelines, expecting reports every 90 days. Outcomes plan must include details of the methodology used for determining the impact of the program and should clearly link to the identified practice gap that the educational activity is designed to address. Outcomes methodology must be appropriate to the proposed activity and the intended goals of the project.
EVALUATION CRITERIA Proposals will be evaluated based on:
• Alignment with identified educational gaps and strategic priorities
• Scientific rigor and independence
• Innovation in educational design and learner engagement
• Strength of outcomes framework and measurable impact
BUDGET Grants request must be under $150,000. Priority will be given to lower cost programs that can deliver the education in a timely manner.
This is the most important predictor.
J&J funding is highly program-specific. A successful application should directly match:
For example, J&J's current educational RFPs specify particular disease areas and learning needs rather than accepting unrestricted research proposals.
Strong proposals demonstrate a clear problem that needs to be solved, such as:
The stronger and more clearly documented the unmet need, the more compelling the proposal.
Innovation is particularly important for J&J's technology and entrepreneurship programs.
Competitive projects may involve:
The Polyphonic AI Fund for Surgery QuickFire Challenge, for example, is specifically designed to accelerate next-generation AI solutions for surgery.
Strong applications clearly explain how the project could:
J&J's current corporate strategy emphasizes addressing complex health challenges through medicines and medical technologies.
Competitive proposals should provide:
For educational grants, the proposal should clearly establish the identified educational gap, proposed intervention, target audience, and expected outcomes.
This is particularly important for J&J educational and implementation grants.
Successful proposals should specify measurable outcomes such as:
For example, a current J&J implementation-science RFP requires reporting on educational reach, learner outcomes, clinician behavior/practice changes, and system/process outcomes.
J&J favors solutions that can move beyond a small pilot.
Competitive projects demonstrate:
This is especially relevant to implementation-science and technology programs.
Competitive teams may include:
J&J Innovation explicitly works with external innovators and provides resources and collaboration opportunities through its innovation ecosystem.
For medical education grants, the application should clearly identify:
J&J's educational grants can support activities delivered through live, virtual, and healthcare-team engagement formats.
Successful proposals should have:
For example, J&J's 2026 implementation-science RFP specifies a maximum award of $275,000, a project duration of up to 18 months, and restrictions on certain expenses.
CME/CE applicants must fall into one of the following categories with a bona fide interest in managing and or treating patients with RRMM: Academic institutions (medicine, pharmacy or nursing), Teaching hospitals, Medical Societies, Professional Associations, Government agencies, medical education companies. Requests must be certified for CME/CE credit(s). Individual physicians or physician owned entities are ineligible to apply. Grants will not be awarded to ex-US entities. This is for US only organizations. APPLICATIONS MUST BE SUBMITTED BY THE ACCREDITED PROVIDER.
It is understood that the accredited provider will comply with all applicable accreditation standards and governing CME/CE requirements, including those of the relevant accrediting body or bodies, as well as applicable federal and state laws and regulations. Applicants will have to identify the accrediting organization(s), credit type(s), and processes that will be used to ensure ongoing compliance throughout the activity lifecycle. You will be required to show proof of accreditation in the required upload section.
Sponsor Institute/Organizations: Johnson & Johnson
Sponsor Type: Corporate/Non-Profit
Address: 1 Johnson & Johnson Plaza, New Brunswick, NJ 08933
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Aug 31, 2026
$150,000
Affiliation: Johnson & Johnson
Address: 1 Johnson & Johnson Plaza, New Brunswick, NJ 08933
Website URL: https://www.jnj.com/innovativemedicine/us/download/Hematology%20Request%20for%20Proposals%20(RFP)
Disclaimer:It is mandatory that all applicants carry workplace liability insurance, e.g., https://www.protrip-world-liability.com (Erasmus students use this package and typically costs around 5 € per month - please check) in addition to health insurance when you join any of the onsite Trialect partnered fellowships.