Apply to the Translational Research Program (TRP)
The goal of translational research is to reduce the time between laboratory findings and actual treatment.
TRP is currently open for submissions.
The Translational Research Program (TRP) was formed to enhance the transfer of basic research findings to clinical usefulness.
We are looking for applications that propose novel approaches to the prevention, diagnosis, or treatment of hematological malignancies and related pre-malignant conditions. Proposals should be based on molecular, cellular, or integrated systems findings and be conceptually innovative and with a clear plan for the eventual clinical translation of the studies proposed and the results expected.
Click here to see our active TRP portfolio.
Please note these important changes to the TRP (Translational Research Program) Program. The 2026 TRP Grant application process has been changed.
The TRP Grant program is geared towards translational medicine for blood cancers. Earlier work in the translational environment has been funded in the past through the TRP mechanism, however, these types of projects would be a better fit for our Discovery Grant program and applicants are directed to apply under that mechanism.
For the 2026 application cycle we will only consider applications that adhere to the following submission guidelines:
- For small molecule compounds the application must have in vivo proof of concept (POC) in appropriate mouse models. Alternatively, based on the mechanism of action, an in vitro POC with patient-derived samples may be considered.
- For cellular or immunotherapies, in vivo POC would make for a stronger application. We acknowledge, however, that depending on the type of therapy being developed an in vitro POC may be more appropriate or necessary.
Applications that don’t meet these criteria should not submit a Letter of Intent for consideration.
Request For Proposal Information
Special Topic of Interest (Large Granular Lymphocytic Leukemia (LGL):
LGL leukemia is a type of chronic leukemia affecting lymphocytes that are part of the immune system. LGL leukemia is characterized by enlarged cells, containing noticeable granules, which can be seen under microscopic examination. There are two types of LGL leukemia: T-cell (T-LGL) and natural killer cell (NK-LGL). Each type may be chronic or aggressive. LGL is a rare disease with a frequency of about 1 in 1 million people. LGL leukemia affects both men and women, and the median age at diagnosis is 60 years.
Indolent LGL leukemia may involve a “watch and wait” approach. If intervention is required therapies are available but most are older, non-targeted approaches and are generally not curative. Better therapies are needed especially for aggressive and refractory disease.
Therefore, LLS is issuing a special callout for projects to develop novel therapies to address LGL leukemia.
Topics of interest include:
- Personalized medicine approach for cancer treatment. Advances in cancer care have significantly improved the lives of patients with hematologic diseases such as AML, CLL, Hodgkin and Non-Hodgkin Lymphomas, MM, and ALL. LLS believes that, with time, cures can be achieved for certain diseases or subtypes of diseases. Therefore, LLS will continue to support research that may revolutionize cancer care for any hematologic disease.
- Development of novel therapies and/or novel therapeutic strategies including those that target mutational and epigenetic events both in the tumor cells and within the microenvironment. Such therapies can be applicable to any hematologic malignancies, but emphasis is warranted in the following areas:
a) Aggressive subtypes of Non-Hodgkin Lymphoma including but not limited to DLBCL, tFL, MCL, PTCL, and ALCL
b) Indolent lymphoma, including but not limited to: CLL, FL, WM (therapies with the potential to provide significant extension of lives of patients or total disease control in defined subtypes)
c) Myeloid disorders including MPN/MDS/AML as well as lymphoid disorders such as ALL
d) Multiple Myeloma and pre-emergent conditions - Improvements in the safety and efficacy of stem cell transplantation.
- LLS is especially interested in novel immunotherapy approaches and understanding novel immune synapses relevant to blood cancers.
- TRP is interested in focusing on diseases of high unmet need. These can include aggressive diseases or diseases that lack effective therapies.
How to apply
- Please refer to the Guidelines & Instructions document above
- Is this your first time applying for an LLS Research grant? You can get started by requesting a new account in the LLS Research Portal by clicking here.
- See the table below for all the key dates and deadlines:
2025-2026 Application Key Dates
Phase | Date |
---|---|
Call for Proposals | July 1, 2025 |
Letter of Intent Due | October 16, 2025 |
Full Application Due | January 23, 2026 |
Panel Review Meetings | March 2026 |
Award Notification* | May 2026 |
Award Start Date | July 1, 2026 |
*LLS' non-negotiable funding agreement terms & conditions are available for download above
Frequently Asked Questions
Are corporate entities allowed to apply?
May I submit more than one application?
If I have an existing TRP award, can I apply for a second?
Can I apply as a PI on one application and a Co-PI on another application?
Should Collaborators and Co-PIs conduct their research at the same institution as the PI?
Should my proposal be responsive to the request for proposals (RFP) topics?
Could this grant cover any subcontract costs?
Why is my administrative officer’s name missing from the online application dropdown menu?
Why can't I delete a document I upload?
Can I adjust the margins and font on the Project Description template?
Do character limits include spaces?
More Questions?
Please refer to the downloadable Guidelines and Instructions document above for answers and for contact information.