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R01AI196477

Project Grant

Overview

Grant Description
IDENTIFICATION AND CHARACTERIZATION OF NOVEL ANTIFUNGALS AGAINST CRYPTOCOCCUS SPP - CRYPTOCOCCUS NEOFORMANS AND CRYPTOCOCCUS GATTII ARE MAJOR FUNGAL PATHOGENS THAT CAUSE SEVERE INFECTIONS, INCLUDING CRYPTOCOCCAL MENINGITIS, PARTICULARLY IN IMMUNOCOMPROMISED INDIVIDUALS. THE WORLD HEALTH ORGANIZATION (WHO) HAS IDENTIFIED C. NEOFORMANS AS ONE OF THE TOP FOUR HIGHEST CRITICAL PRIORITY FUNGAL PATHOGENS DUE TO ITS SUBSTANTIAL DISEASE BURDEN, INCREASING DRUG RESISTANCE, AND THE LACK OF EFFECTIVE THERAPIES. EVEN WITH AVAILABLE TREATMENTS, THE MORTALITY RATE FOR CRYPTOCOCCAL MENINGITIS OFTEN EXCEEDS 50%, HIGHLIGHTING THE URGENT NEED FOR NEW THERAPEUTIC STRATEGIES. DIHYDROOROTATE DEHYDROGENASE (DHODH), A PIVOTAL ENZYME IN THE DE NOVO PYRIMIDINE BIOSYNTHESIS PATHWAY, IS A PROMISING ANTIFUNGAL TARGET DUE TO ITS ESSENTIAL ROLE IN FUNGAL SURVIVAL. THE SUCCESS OF OLOROFIM, A SELECTIVE DHODH INHIBITOR EFFECTIVE AGAINST ASPERGILLUS FUMIGATUS, UNDERSCORES THE THERAPEUTIC POTENTIAL OF TARGETING DHODH. HOWEVER, OLOROFIM IS INEFFECTIVE AGAINST C. NEOFORMANS AND C. GATTII, LIKELY DUE TO STRUCTURAL AND SEQUENCE DIFFERENCES IN THEIR DHODHS. IMPORTANTLY, STUDIES HAVE SHOWN THAT PYRIMIDINE BIOSYNTHESIS IN C. NEOFORMANS IS VITAL FOR SURVIVAL, AS SERUM AND CELLULAR PYRIMIDINE LEVELS ARE INSUFFICIENT TO BYPASS DHODH INHIBITION. THIS MAKES CNEDHODH AN ATTRACTIVE AND ACTIONABLE TARGET FOR ANTIFUNGAL DRUG DEVELOPMENT. THIS PROPOSAL FOCUSES ON DEVELOPING SELECTIVE INHIBITORS OF CNEDHODH TO ADDRESS THE CRITICAL THERAPEUTIC GAP FOR CRYPTOCOCCAL INFECTIONS. HIGH-THROUGHPUT SCREENING (HTS) WILL BE CARRIED OUT TO IDENTIFY INHIBITORS FROM LARGE COMPOUND LIBRARIES. IDENTIFIED HITS WILL BE VALIDATED FOR POTENCY, SELECTIVITY AGAINST HUMAN DHODH, AND ANTIFUNGAL ACTIVITY AGAINST C. NEOFORMANS AND OTHER CLINICALLY RELEVANT PATHOGENS. ITERATIVE MEDICINAL CHEMISTRY WILL OPTIMIZE LEAD COMPOUNDS TO IMPROVE THEIR PHARMACOKINETICS, POTENCY, AND SELECTIVITY. STRUCTURAL STUDIES, INCLUDING CO-CRYSTALLIZATION AND MOLECULAR MODELING, WILL PROVIDE DETAILED INSIGHTS INTO INHIBITOR BINDING, ENABLING RATIONAL DRUG DESIGN. FINALLY, OPTIMIZED COMPOUNDS WILL BE TESTED IN ANIMAL MODELS OF C. NEOFORMANS INFECTION TO EVALUATE THEIR IN VIVO EFFICACY, PHARMACOKINETICS, AND SAFETY. THE DEVELOPMENT OF CNEDHODH INHIBITORS WILL ADDRESS A CRITICAL UNMET NEED FOR EFFECTIVE ANTIFUNGAL THERAPIES FOR CRYPTOCOCCAL INFECTIONS WHILE EXTENDING THE APPLICABILITY OF DHODH AS A DRUG TARGET TO FUNGAL PATHOGENS BEYOND A. FUMIGATUS. THIS WORK HAS THE POTENTIAL TO TRANSFORM THE TREATMENT OF INVASIVE FUNGAL INFECTIONS CAUSED BY CRYPTOCOCCUS SPP., SIGNIFICANTLY IMPROVING OUTCOMES FOR VULNERABLE PATIENTS. BY LEVERAGING INNOVATIVE SCREENING APPROACHES, STRUCTURAL INSIGHTS, AND MEDICINAL CHEMISTRY, THIS PROJECT AIMS TO DELIVER NOVEL ANTIFUNGAL AGENTS THAT COULD SAVE LIVES AND REDUCE THE GLOBAL BURDEN OF CRYPTOCOCCAL INFECTIONS.
Funding Goals
<P>THE GOALS ARE:</P><UL><LI>TO FOSTER FUNDAMENTAL CREATIVE DISCOVERIES, INNOVATIVE RESEARCH STRATEGIES, AND THEIR APPLICATIONS AS A BASIS FOR ULTIMATELY PROTECTING AND IMPROVING HEALTH;</LI><LI>TO DEVELOP, MAINTAIN, AND RENEW SCIENTIFIC HUMAN AND PHYSICAL RESOURCES THAT WILL ENSURE THE NATION'S CAPABILITY TO PREVENT DISEASE;</LI><LI>TO EXPAND THE KNOWLEDGE BASE IN MEDICAL AND ASSOCIATED SCIENCES IN ORDER TO ENHANCE THE NATION'S ECONOMIC WELL-BEING AND ENSURE A CONTINUED HIGH RETURN ON THE PUBLIC INVESTMENT IN RESEARCH; AND</LI><LI>TO EXEMPLIFY AND PROMOTE THE HIGHEST LEVEL OF SCIENTIFIC INTEGRITY, PUBLIC ACCOUNTABILITY, AND SOCIAL RESPONSIBILITY IN THE CONDUCT OF SCIENCE.</LI></UL><P>IN REALIZING THESE GOALS, THE NIH PROVIDES LEADERSHIP AND DIRECTION TO PROGRAMS DESIGNED TO IMPROVE THE HEALTH OF THE NATION BY CONDUCTING AND SUPPORTING RESEARCH:</P><UL><LI>IN THE CAUSES, DIAGNOSIS, PREVENTION, AND CURE OF HUMAN DISEASES;</LI><LI>IN THE PROCESSES OF HUMAN GROWTH AND DEVELOPMENT;</LI><LI>IN THE BIOLOGICAL EFFECTS OF ENVIRONMENTAL CONTAMINANTS;</LI><LI>IN THE UNDERSTANDING OF MENTAL, ADDICTIVE AND PHYSICAL DISORDERS; AND</LI><LI>IN DIRECTING PROGRAMS FOR THE COLLECTION, DISSEMINATION, AND EXCHANGE OF INFORMATION IN MEDICINE AND HEALTH, INCLUDING THE DEVELOPMENT AND SUPPORT OF MEDICAL LIBRARIES AND THE TRAINING OF MEDICAL LIBRARIANS AND OTHER HEALTH INFORMATION SPECIALISTS.</LI></UL>
Place of Performance
Arizona United States
Geographic Scope
State-Wide
University Of Arizona was awarded Developing CNEDHODH Inhibitors for Cryptococcus spp. Project Grant R01AI196477 worth $3,100,997 from the National Institute of Allergy and Infectious Diseases in June 2026 with work to be completed primarily in Arizona United States. The grant has a duration of 4 years and was awarded through assistance program 93.855 Allergy and Infectious Diseases Research. The Project Grant was awarded through grant opportunity NIH Research Project Grant (Parent R01 Clinical Trial Not Allowed).

Status
(Ongoing)

Last Modified 6/5/26

Period of Performance
6/5/26
Start Date
5/31/30
End Date
0% Complete

Funding Split
$3.1M
Federal Obligation
$0.0
Non-Federal Obligation
$3.1M
Total Obligated
100.0% Federal Funding
0.0% Non-Federal Funding

Activity Timeline

Interactive chart of timeline of amendments to R01AI196477

Additional Detail

Award ID FAIN
R01AI196477
SAI Number
R01AI196477-1572604686
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Public/State Controlled Institution Of Higher Education
Awarding Office
75NM00 NIH National Institute of Allergy and Infectious Diseases
Funding Office
75NM00 NIH National Institute of Allergy and Infectious Diseases
Awardee UEI
ED44Y3W6P7B9
Awardee CAGE
0LJH3
Performance District
AZ-90
Senators
Kyrsten Sinema
Mark Kelly
Modified: 6/5/26