SBIR/STTR Research Award

Phase 2 Selective DAT inhibitor for treatment of Obesity.

Award identifier d384b7847afac8e4ce379b42087570128b1c76a7b4815d8e7807967c38dfeaa4Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$1,510,798

Program and phase

SBIR · Phase II

Award year

2011

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
P2D, INC
Proposal award date
Not reported
Contract end date
Not reported
UEI
KX3EAX2JEMV8
Solicitation number
PA10-050
Topic code
NIDDK

Research abstract

DESCRIPTION (provided by applicant): PD2007 is a selective DAT inhibitor that P2D Bioscience (P2D) is developing for the treatment of obesity. PD2007 is an analog of benztropine (Cogentin) a non-Scheduled, safe FDA-approved drug in clinical use for over 40years. Structure-activity-relationship studies were conducted to improve PD2007 efficacy while decreasing side-effects. Our SBIR Phase 1 data demonstrate that PD2007 produces sustained weight-loss and decreased body fat. PD2007 appears to decrease body weight by increasing energy expenditure, a novel mechanism of action. PD2007 is radically different from the non-selective DAT inhibitor, amphetamine, a potent anti-obesity drug: For example: 1. PD2007-induced weight-loss appears due to increased energy expenditure unlike the appetite suppressant amphetamine 2. PD2007 is not addicting; amphetamine is an addicting Schedule II drug of abuse 3. PD2007 does not affect blood pressure or heart rate; amphetamine significantly increases both 4. PD2007 is not a stimulant; amphetamine is a widely used stimulant 5. PD2007's pharmacokinetics are consistent with once a day dosing while amphetamine requires multiple daily dosing for efficacy. The purpose of the proposed SBIR Phase 2: 1) Aim 1 will further assess whether PD2007 has a novel mechanism of action in inducing weight-loss - enhanced energy expenditure, and 2) Aims 2, 3, 4 and 5 represent preclinical safety studies responsive to FDA-guidance ICH M3 for the successful submission of a PD2007 Investigational New Drug(IND) application. This IND would allow clinical testing of PD2007 in humans. Specifically: Aim 1: Determine if PD2007-induced weight-loss is associated with increased energy expenditure, lipolysis and/or glycogenolysis. Aim 2: Assess PD2007 genotoxicity.Aim 3: Assess PD2007 absorption, distribution, metabolism and excretion (ADME). Aim 4: Assess oral PD2007 safety pharmacology in three studies. Aim 5: Assess repeated PD2007 dose toxicity in rats. PUBLIC HEALTH RELEVANCE: In the present application,we propose preclinical studies to determine if PD2007, our anti-obesity drug, has a novel mechanism of action. PD2007 appears to increase energy expenditure and general activity rather than the standard weight-loss method of suppressing appetite. By increasing energy expenditure and general activity, PD2007 would be a healthier way to lose weight. Also, preclinical safety studies will be performed that are required by the US Food and Drug Administration (FDA). These studies, once completed, will allow thestudy of PD2007 for the first time in humans including those with obesity.

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

52 SBIR/STTR records share this UEI (2001–2021). Reported award amounts total $21,593,440. 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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