SBIR/STTR Research Award

AVM0703 combined with Non-Hodgkin's Lymphoma standard of care to enhance complete response rates without additional toxicities

Award identifier e93a1440694d79f559413a0b36b9a8e67cc1a1ffbc1e05cf1fc8f7502c090a57Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$399,193

Program and phase

SBIR · Phase I

Award year

2022

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
AVM BIOTECHNOLOGY, INC.
Proposal award date
2022-08-05
Contract end date
2023-07-31
UEI
D29NFMS3DJJ8
Solicitation number
PA21-259
Topic code
102

Research abstract

PROJECT SUMMARY Non-Hodgkin’s Lymphoma (NHL) represents 4% of all cancer diagnosed in the U.S., and as many as 50% of patients will relapse within 2 years of diagnosis and treatment. The current standard of care is chemotherapy. For Diffuse Large B cell Lymphoma subtype (DLBCL) CHOP (cyclophosphamide- doxorubicin-vincristine-prednisone) is given in combination with an anti-CD20 monoclonal antibody, such as rituximab (R-CHOP). Unfortunately, chemotherapy requires numerous treatment cycles with challenging side effects and does not completely remove the cancerous lymphocytes, as indicated by the frequency of relapse. A drug that could reduce the lymphoma population and essentially increase the potency of the chemotherapy regimen (fewer lymphoma cells to the chemotherapy concentration) would have the potential to be synergistic as a treatment strategy. AVM0703, a proprietary formulation of high concentration dexamethasone developed by AVM Biotechnology, has been shown to control NHL growth in murine models. It also safely reduces lymphocytes following a single very high dose via one-hour infusion, in both pre-clinical and clinical settings. AVM0703 is currently the subject of a US-based clinical study in no-option, relapsed/refractory NHL patients and is distinguished from other investigative drugs in this ‘terminal no-option’ patient population by its absence of safety concerns with patients reporting feeling great, regaining appetite and energy, and durable response recorded. The goal of this project is to validate the combination of AVM0703 and standard DLBCL chemotherapy R-CHOP. This approach is expected to increase complete response rates and potentially reduce the required number of chemotherapy cycles, providing a more tolerable therapeutic option for newly diagnosed NHL patients. The feasibility of this approach will be validated in Phase I with the following aims: Aim 1) Evaluate the ability of AVM0703 in combination with R-CHOP to reduce R-CHOP cycles in an aggressive, immune-resistant murine B cell NHL model. Aim 2) Assessment of AVM0703 combination therapy with reduced dose R-CHOP to enhance outcomes in elderly patients. The Phase II project will further focus on efficacy studies, and a small clinical trial with newly diagnosed NHL patients to evaluate the effects of this novel therapeutic treatment approach.

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

6 SBIR/STTR records share this UEI (2019–2025). Reported award amounts total $5,458,747. Reported amounts are not federal obligations.

Phases: Phase I, Phase II, Phase II – Direct to Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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