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Small Business Program

Division of AIDS High-Priority Areas of Interest

NIAID encourages applications in the areas of HIV/AIDS prevention and treatment. The mission of Division of AIDS (DAIDS) is to help ensure an end to the HIV/AIDS epidemic by increasing basic knowledge of the pathogenesis and transmission of the human immunodeficiency virus (HIV); supporting the development of therapies for HIV infection and its complications and co-infections; and supporting the development of vaccines and other prevention strategies.

Below are areas of interests from DAIDS. The subject matter expert is available to answer questions and advise on the application process.

If you do not see your HIV/AIDS-related topic here, the application may not be prioritized but will still be reviewed. Contact Daniella Livnat or Natalia Kruchinin if you have any questions about your application and don’t see an appropriate subject matter expert below.

Areas of Interest

Subject Matter Experts

Research to assess and overcome specific biomedical obstacles in HIV vaccine discovery, especially by application of novel technology to vaccine discovery and/or by the development and supply of novel reagents and other resources useful in novel vaccine discovery. Stuart Shapiro
Preclinical Research and Development Branch

Preclinical development and evaluation of HIV vaccines, adjuvants, and delivery systems in animal models using SIV, SHIV, or HIV.

Vaccines that enhance innate and mucosal immunities and induce broadly reactive and long lasting neutralizing antibodies are program priorities.

Novel technologies (e.g., nanotechnology) and vaccine vectors are also priority areas of research interest.

Yen Li
Preclinical Research and Development Branch

Translational research to facilitate advancing novel promising basic SIV/HIV vaccine research concepts into HIV vaccine products, including: 1) vector optimization for expression, safety, and manufacturability; 2) upstream and downstream development activities; 3) analytics development to support in process testing and release; 4) formulation development; 5) novel adjuvant approaches; 6) GMP manufacturing; and 7) preclinical safety and toxicology modeling.

Jeffrey K. Pullen
Vaccine Translational Research Branch

Development of rapid diagnostic tests to distinguish HIV-vaccinated and HIV-infected individuals. HIV Env immunogens formulated with immunological adjuvant(s): Development of assays to ensure proper formulation, antigen/adjuvant integrity and potency, and characterization of immunological space post-vaccination. Evaluation and monitoring of vaccine safety and efficacy by identifying biomarkers of safety, autoimmunity, inflammation and immunogenicity.

Jim Lane
Vaccine Clinical Research Branch

Preclinical development of single and combination non-vaccine biomedical prevention candidates (topical microbicides, PrEP and multipurpose prevention technologies (MPT)) which prevent the transmission of HIV in the genital and gastrointestinal tracts of men and women.

Development of oral, injectable, implantable, and topical sustained delivery strategies for topical microbicides, PrEP, and MPT.

Creation and advancement of new technologies, targets, and approaches, including nanotechnology, which promote the safety, efficacy, adherence, and acceptability of non-vaccine biomedical prevention candidates and strategies.

Jim A. Turpin
Preclinical Microbicide and Prevention Research Branch

Discovery and development of agents or strategies for pre-exposure prophylaxis (PrEP) (single or multiple agents, immunological, pharmacological, or other potential approaches directed against viral and/or host targets). Development of pharmacological tools to examine PK/PD in fluids and tissue, new formulation and delivery systems (including nanotechnology-based approaches) for coitally dissociated use, and optimization of animal models for screening of candidate agents.

David Burns
Clinical Prevention Research Branch

Development of novel assay for the determination of HIV incidence.

These diagnostic assays should identify HIV incidence in the first year of infection, be based on B and non-B subtypes, differentiate those with early vs. chronic HIV infection and latent infection; and include the development, incorporation, and validation of process controls.

Usha Sharma
Clinical Prevention Research

Development of formulation strategies to deliver antiretrovirals to specific target cells or tissues.

Development of sustained release formulations to be delivered by oral, injectable, implantable, or transdermal routes of administration for treatment of HIV infection.

Steve Turk
Drug Development and Clinical Sciences Branch

Preclinical discovery and development of antimicrobial agents directed against Mycobacterium avium, Mycobacterium abscessus, Pneumocystis Pneumonia, and Cryptococcus neoformans (and other pathogenic fungi).

Development and delivery of nanotechnology-based therapeutics to target pathogen or pathogen-infected cells.

Influence of antiretrovirals (e.g., ritonavir) on antimicrobial efficacy.

Chris Lambros
Complications and Coinfections Research Branch

Small molecule inhibitors of viral and cellular targets not yet covered by FDA-approved antiretrovirals; HIV therapeutics discovery including high-throughput screening; development of nanotechnology-based therapeutics; HIV gene therapies, including vector design; animal models for HIV therapeutics and cure strategies.

Brigitte Sanders
Targeted Interventions Branch

HIV therapeutic vaccines, monoclonal antibody discovery and development for therapeutic use; immune-based HIV cure strategies; assays to measure the latent HIV reservoir

Tony Conley
Targeted Interventions Branch

Development of novel methods for the diagnosis of active and latent TB infection in HIV-positive or HIV-negative infants and children.

Development of prognostic biomarkers for risk of development of active TB and prediction of treatment response.

Lakshmi Jayashankar
Contractor, Henry M. Jackson Foundation

Development and evaluation of practical and affordable tests to measure viral load, drug toxicities, and drug resistance to monitor populations in resource-poor settings.

Development of tests to detect early infection in seropositive HIV-infected adult and pediatric individuals

Joseph Fitzgibbon
Drug Development and Clinical Sciences Branch

Development of rapid tests for the detection of ARTs in various human matrices (e.g. blood, urine, hair).

The assay should require minimal operator effort and expertise, and include the development, incorporation, and validation of process controls.

Hao Zhang
Drug Development and Clinical Sciences Branch

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Last Updated July 31, 2015

Last Reviewed May 01, 2014