SBIR/STTR Research Award

Botanical Drug for Chemotherapy Induced Nausea and Vomiting

Award identifier b2aebf40d81cb9cfc339f8090af88ec8fc267f8cfffcae9965effe548dd6de7dAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$416,134

Program and phase

SBIR · Phase I

Award year

2025

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Aphios Corporation
Proposal award date
2025-09-01
Contract end date
2026-08-31
UEI
HDE2J1H521A7
Solicitation number
PA24-245
Topic code
NCCIH

Research abstract

PROJECT SUMMARY Nausea and vomiting are among the most distressing side effects of chemotherapy. This unmet need is acute in the adult and pediatric populations undergoing chemotherapy and is the reason why up to 50% of patients refuse subsequent chemotherapy treatment. Despite the widespread use of the 5-HT3 and NK-1 receptor antagonist antiemetics, chemotherapy induced nausea and vomiting (CINV) continues to be reported by up to 70% of adult patients receiving highly emetogenic chemotherapy agents. These synthetic antiemetics are expensive and burdened with significant side effects. Additionally, an off-label anti-psychotic olanzapine is finding frequent use as a rescue medication despite its serious adverse side effects. There is a high unmet need for improved products to treat CINV without adverse side effects. To meet this unmet medical need, we are developing a botanical drug based on ginger which has been used for centuries, from Aisa to Egypt and North America to manage gastrointestinal stress. The overall goal of this proposal is to develop a highly purified and standardized ginger product, Zindol, as a botanical drug product for the treatment of CINV. In Phase I, we plan to develop and manufacture an improved, highly purified active pharmaceutical ingredient (API) of Zingiber Officinale as well as a formulated drug product (FDP) in gelatin capsules, characterize these products, conduct stability studies and establish release criteria. We will also perform an innovative in vitro nausea assays to define and control manufacturing. In Phase II, we will scale manufacturing, conduct IND-enabling in vivo toxicology and pharmacology GLP studies, meet with the FDA and establish the regulatory pathway for conducting clinical trials. In Phase III, we plan to conduct clinical trials on Zindol® for the treatment of nausea and emesis in adults undergoing chemotherapy, and license the botanical drug with strategic corporate partners to address the $3.4B marketplace.

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

44 SBIR/STTR records share this UEI (1994–2025). Reported award amounts total $17,170,079. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services, National Science Foundation, Department of Defense

Agency intelligence

Department of Health and Human Services

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