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Translational Research Program (TRP)

Apply Here: https://lls.fluxx.io

Please reach out to [email protected] with any questions.

 

TRP 2025/2026 cycle is currently open.

Please submit a Letter of Intent.

Since 1995, the Translational Research Program grants fund new and innovative research that shows high promise of moving from laboratory discoveries to clinical application.

The goal of this translational award is to reduce the time between laboratory findings and actual treatment, putting research on the bench-to-bedside fast track when it comes to finding better treatment and cures for blood cancers.

Find out more about the application process or browse resources for current awardees below. 


Meet some of our recent grantees:

Headshot of Dr. Aditi Shastri, Associate Professor of Medicine (Oncology)

"The Leukemia & Lymphoma Society TRP grant funding has been truly transformative for me and has been a major stepping stone in my career as a physician-scientist. The philosophy of LLS closely aligns with our patients' greatest need. I am very inspired by LLS and the wonderful people that work here! In our TRP grant we further study the role of STAT3 and its upregulation in leukemic stem cells. We are testing combinations of FDA approved drugs with a novel antisense inhibitor of STAT3 in therapy resistant cell lines. Our greatest hope is to be able to provide more therapeutic options for our patients with relapsed/refractory hematologic malignancies."

Aditi Shastri, MBBS
Albert Einstein College of Medicine

Antisense inhibition of STAT3 as a therapeutic strategy against leukemic stem cells

"The Leukemia and Lymphoma Society is a funding agency that has really transformed the field of hematopoietic malignancies by targeting adequate funding to exciting and challenging basic research and translational projects. In this project we are attempting to target stress response in pediatric T-cell leukemia (T-ALL), and LLS funding will let us develop genetic tools and test compound combinations, that will hopefully lead to a future clinical trial."

Iannis Aifantis, PhD
NYU Langone Health

Targeting the stress response machinery in pediatric T cell acute lymphoblastic leukemia (T-ALL)

"The Leukemia & Lymphoma Society has generously supported our research program in hematological malignancies for many years. This new Translational Research Program award is based on our discovery that a sizable subset of follicular lymphomas activates a pathway called autophagy that allows for tumor cell survival under limited nutrient conditions. Such stressful starvation conditions are postulated to exist in crowded enlarged lymph nodes or other organs infiltrated with lymphoma. With support from this grant we are trying to understand additional aspect of this survival mechanism, which we hope will inform us on novel strategies to treat follicular lymphoma. To develop such novel treatments, we are commencing with screens to identify new compounds that inhibit autophagy and aim at developing a clinical trial that will target activated autophagy as a vulnerability in follicular lymphoma."

Sami Malek, MD
University of Michigan Rogel Cancer Center

Targeting v-ATPase mutations and activated autophagic flux in follicular lymphoma

Headshot of Soheil Meshinchi, PhD MD who is an award recipient

"I am very grateful to The Leukemia & Lymphoma Society for awarding me with this Translational Research Program grant. This critical funding will help our team advance targeted and immunotherapeutic treatments for infants and babies under the age of five with subtypes of acute leukemia who do not respond to standard chemotherapy. We hope that this work will lead to therapies that can cure this aggressive type of leukemia without harming the infants’ growing bodies."

Soheil Meshinchi, MD, PhD
Fred Hutchinson Cancer Research Center

Novel immunotherapeutic strategies in infants with high risk AML

"I am immensely grateful to receive the LLS funding because it will allow us to shine a light on a critically important mechanism whereby cancer genes are activated and deactivated by changes in the overall structure of the DNA. This type of gene deregulation is brought about by movement of DNA from one chromosome to another leading to cancer gene overexpression by relocation of gene control elements and changes in nuclear DNA organization. Importantly these events can be complex leading to the deregulation of more than one gene simultaneously, which can explain rapid changes in cancer behavior and suggest new ways of predicting how aggressive the cancer will be."

Gareth J. Morgan, MD, PhD, MBBCh, FRCP, FRCPath
NYU Langone Health

Structural Chromosomal Rearrangements and the Multi-Step Progression of Multiple Myeloma

"I am very honored to receive this award from The Leukemia & Lymphoma Society. These funds will support the development of the liquid biopsy as a diagnostic tool in Hodgkin lymphoma. An unmet medical need in Hodgkin lymphoma, the second most common aggressive lymphoma type, is the early and accurate identification of chemorefractory patients, as they are candidates for treatment intensification to maximize the chances of cure, as well as the early and accurate identification of good-risk patients, as they are candidates for treatment de-escalation to avoid both short and long-term complications of chemo-radiotherapy. If successful, the project will provide an innovative, non-invasive and radiation-free tool for improving disease response assessment in Hodgkin lymphoma. "

Davide Rossi, PhD, MD
Foundation for the Institute of Oncology Research (IOR)

Treatment tailoring by optimized early residual disease assessment in classic Hodgkin lymphoma

Headshot of Dr. Ashwin Unnikrishnan, Cancer Researcher

"I am honoured and delighted to receive the prestigious Translational Research Program grant from The Leukemia & Lymphoma Society. This generous support will support our aim to develop more effective treatments for Myelodysplastic Syndromes (MDS), a disease that is increasing in prevalence given rapidly aging populations worldwide. The best available treatment option for many MDS patients is the drug 5-azacitidine. However, it is only effective in about half of the patients who are treated and the prognosis is poor for those who fail to respond to treatment. In addition, most of those patients who initially respond to treatment will eventually relapse. There is therefore a need to develop new treatment options that will be more effective and durable. With the generous support of the LLS, we aim to pursue some tantalizing leads we have recently uncovered that might shine a light on the path forward towards this eventual goal."

Ashwin Unnikrishnan, PhD
University of New South Wales

Beyond Azacitidine: Investigating new therapeutic strategies for the treatment of MDS

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.

See our active TRP portfolio.

Please find all TRP program documents available for download here:

2025 TRP Guidelines and Instructions (PDF)
TRP Funding Agreement Template – FY25 (PDF)

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, Blood Cancer United 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. Blood Cancer United believes that, with time, cures can be achieved for certain diseases or subtypes of diseases. Therefore, Blood Cancer United 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.
  • Blood Cancer United 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 and Instructions document above
  • Is this your first time applying for an Blood Cancer United Research grant? You can get started by requesting a new account in the Blood Cancer United Research Portal.
  • See the table below for all the key dates and deadlines: 

2025-2026 Application key dates

PhaseDate
Call for ProposalsJuly 1, 2025
Letter of Intent DueOctober 16, 2025
Full Application DueJanuary 23, 2026
Panel Review MeetingsMarch 2026
Award Notification*May 2026
Award Start DateJuly 1, 2026

Blood Cancer United's non-negotiable funding agreement terms & conditions are available for download above

Frequently asked questions

The Policies and Procedures are available to download from the TRP webpage or from the Blood Cancer United Research Portal (FLUXX) program information pages.

Are corporate entities allowed to apply?

No. Only academic institutions are eligible to receive funds from Blood Cancer United Research Grants. Applicants from the National Institutes of Health or other government agencies are also not eligible. Corporations conducting blood cancer research are, however, encouraged to inquireabout our venture philanthropy initiative, the Therapy Acceleration Program (TAP).

How is independence defined?

Independence is defined as an academic appointment or similar non-corporate position that has sole responsibility for directing research and funding the work. Usually this means a professor, associate or assistant professor or an equivalent appointment. Post-doctoral and similar appointments are not considered independent positions.

May I submit more than one application?

No. Applicants may only serve as the PI or Co-PI for one new TRP application per cycle.

If I have an existing TRP award, can I apply for a second?

Yes, an investigator may apply for a new TRP if they currently hold an active TRP from a prior year. The proposed work may be a new research objective or may be related to the active TRP but should not directly overlap with the aims of the existing TRP.

Can I apply as a PI on one application and a Co-PI on another application?

No. Applicants may not serve as PI or Co-PI on more than one application within the same cycle. Applicants may, however, serve as Collaborator on more than one application.

Should Collaborators and Co-PIs conduct their research at the same institution as the PI?

Not necessarily. A Co-PI or Collaborator may work at a different institution – or even in a different country – from the PI.

Should my proposal be responsive to the request for proposals (RFP) topics?

Not necessarily. Blood Cancer United seeks proposals that are responsive to the RFP but will consider other exceptional proposals with the near-term potential of clinical translation.

What are permissible costs?

Permissible Direct Costs include salary, wage, or stipend with fringe benefits, supplies and materials, equipment, travel, and patient care costs. Permissible Indirect Costs include those incurred for common or joint objectives that cannot be readily identified with a particular project (general maintenance, utilities, library, etc.), as defined in Office of Management and Budget Circular A-21. Impermissible Costs include membership dues, tuition, books, journals, and publication costs.

Are subcontracts allowed?

Yes. The signing institution (i.e. the Funded Institution) is responsible for academic and CRO subcontracts. Blood Cancer United will only sign a contract with and dispense payments to the Funded Institution and does not facilitate subcontracts.

Could this grant cover any subcontract costs?

Yes. While Blood Cancer United does not facilitate subcontracts, subcontract costs may be claimed as part of the Funded Institution’s direct costs. Indirect costs may only be claimed by one institution (usually the Funded Institution).

Why is my administrative officer’s name missing from the online application dropdown menu?

In order for personnel to be selected from dropdown menus on the application, each individual must have an account in the Blood Cancer United Research Portal (FLUXX) that is linked to the Funded Institution of the application. Please contact [email protected] to request new accounts.

Why can't I delete a document I upload?

In order to avoid accidental deletions, applicants are not granted access to delete uploaded documents. We recommend that all application documents be thoroughly reviewed before they are uploaded. Applicants wishing to correct an uploaded document should contact [email protected] to have the document replaced with a corrected version. Please note that the correction will be apparent to reviewers.

Can I adjust the margins and font on the Project Description template?

No. Applications that are submitted with altered templates will be triaged.

Do character limits include spaces?

Yes. Character limits include spaces throughout all Blood Cancer United grant applications.

What if my Human Subjects and Laboratory Animal assurances haven’t been approved before the application deadline (IRB, IACUC)?

Assurances pending approval should be noted on your application, and approval letters should be uploaded as soon as they are received. Approval letters received after the deadline should be sent to [email protected] as soon as they are received and will be added to your application by Blood Cancer United administrative staff.

Could someone switch labs before the grant start date of July 1st of the year in which the grant is awarded?

Yes. Applicants should alert Blood Cancer United Research Administration of a potential move as soon as possible. The new Funded Institution will be subject to Blood Cancer United approval.

More questions?

Please refer to the downloadable Guidelines and Instructions document above for answers and for contact information.

Get information about other programs, and about applying for Blood Cancer United research funding.


Grant requirements

Reporting Schedule: Progress, IP Disclosure,* Financial, and Conflicts Disclosure** Reports are required for each year of the grant, and Publications Reports are required each quarter. The reporting schedule for your particular grant is printed on your Grant Agreement. This schedule is also available under Reports Due in the Blood Cancer United Research Portal (FLUXX). Below is an example of a typical schedule for a new TRP grant starting on July 1, 2020. The reporting schedule for TRP Renewals, which run in two-year periods, will also follow this pattern, with final reports due in the second year.

Example Reporting Schedule for New TRP Grant 2020
Publications Report #1October 1, 2020
Publications Report #2January 1, 2021
Publications Report #3  April 1, 2021
Interim Year 1 Progress Report
Interim Year 1 IP Disclosure Report*
Interim Year 1 Conflicts Disclosure Report**
  May 1, 2021
Publications Report #4  July 1, 2021
Interim Year 1 Financial Report  September 1, 2021
Publications Report #5  October 1, 2021
Publications Report #6  January 1, 2022
Publications Report #7  April 1, 2022
Interim Year 2 Progress Report
Interim Year 2 IP Disclosure Report*
Interim Year 2 Conflicts Disclosure Report**
  May 1, 2022
Publications Report #8  July 1, 2022
Interim Year 2 Financial Report  September 1, 2022
Publications Report #9  October 1, 2022
Publications Report #10  January 1, 2023
Publications Report #11  April 1, 2023
Publications Report #12  July 1, 2023
Final Progress Report
Final IP Disclosure Report*
Final Financial Report
Final Conflicts Disclosure Report**
  September 1, 2023

*The IP Disclosure Report was formerly referred to as the Patent Report.
**The Conflicts Disclosure Report is an annual requirement for awards activated in 2020 or later.

Report Submission: Blood Cancer United research grant reporting is conducted through the Blood Cancer United Research Portal (FLUXX). Access this portal using the same username and password that were used during the application process. 
Individuals responsible for submitting reports must be manually added to each individual grant record in our system in order for them to have reporting access for each grant. Contact [email protected] to update reporting access for your grant.

Progress Reports and Publications Reports should be submitted by the Grantee/PI. Financial Reports should be submitted by the financial officer, and IP Disclosure Reports should be submitted by the technology/transfer officer. Conflicts Disclosure Reports should also be routed through the technology/transfer office but may be submitted by the PI.

Researchers and administrators should be careful to follow all instructions on the report web form and downloadable template. Reports that fail to follow instructions will be returned for revision, which may delay grant payment. Do not save templates for future use; the templates are subject to change and therefore must be newly downloaded for each submission.

Report Submission Guide (PDF)

Download the Report Submission Guide for detailed instructions on submitting a report in the Blood Cancer United Research Portal (FLUXX).
Note: FLUXX recently updated the grantee portal view, so the pages will visually be different from the screenshots shown in this guide. This change is aesthetic only; the process for submitting reports remains unchanged.

Progress Meeting: During the third year of funding, TRP grantees will be invited to present their research progress to Blood Cancer United Research staff as well as to TRP grantees in the same funding year. This meeting is typically held in the fall in New York City. Grantees working outside of the continental United States will be invited to attend via video conference. Each participant (either the project's PI or a representative) will present the research progress using PowerPoint. Each presentation should last no more than 15 minutes with 5 minutes for questions and answers (maximum slide deck of 10 slides). Blood Cancer United will cover travel expenses for those who choose to attend. Further information regarding this meeting will be sent via email from [email protected] to the PI approximately 6 months prior to the meeting.

Grant payment

Blood Cancer United pays research grants quarterly in March, June, September, and December. Payments are contingent upon reporting requirements; all report approvals must be up to date in order for payment to be processed. A list of sent payments can be viewed in the Blood Cancer United Research Portal (FLUXX) under Dispersed Payments.

Transfers

Blood Cancer United approval is required at least 30 days prior to an award's transfer to a new institution or laboratory. In order to submit a request for transfer, complete a Special Requests report in the Blood Cancer United Research Portal (FLUXX). Your request will be reviewed, and you will receive a notification from Blood Cancer United with the results of the review or with a request for more information. Approval is contingent upon continued research support and sponsorship, fitness of the new research environment, and circumstances of your award type and timing of the request (see your Grant Agreement for more details).

Transfer to another investigator may be allowed if the original grantee is unable to continue the project (e.g. if they move to a new institution unequipped for the project). Contact [email protected] to inquire about a grantee transfer.

Leaves of absence

Blood Cancer United approval is required at least 30 days prior to the interruption of an award. Leaves of absence may not exceed 1 year in duration. In order to submit a request for leave of absence, complete a Special Requests report in the Blood Cancer United Research Portal (FLUXX).  If the request is approved, funding of the award will be suspended during the leave period, and the grant term will be extended for a period equal to the duration of the suspension (e.g. following an approved 1-year leave of absence, an award originally scheduled to end 6/30/2022 will end 6/30/2023).

No-cost extensions

TRP grantees are permitted to request a no-cost extension for a maximum of one year in duration. At the end of the no-cost extension period, any funds remaining must be returned to Blood Cancer United. To request a no-cost extension, complete a Special Requests report in the Blood Cancer United Research Portal (FLUXX). If the request is approved, the grant period will be extended for one year, and final reports will be due 60 days following the new end date. The final payment will be paid once final reports are received and approved by Blood Cancer United.


If you have questions regarding your grant that are not addressed here, please contact the Research Administration Team at [email protected].

The Leukemia & Lymphoma Society (LLS) is now Blood Cancer United. Learn more.