SBIR/STTR Research Award
Mechanism and Therapies for HAART Induced Diarrhea
Award amount
$99,900Program and phase
SBIR · Phase IAward year
2001Award details
- Awarding agency
- Department of Health and Human Services
- Branch
- National Institutes of Health
- Recipient company
- DIGESTIVE CARE, INC.
- Proposal award date
- Not reported
- Contract end date
- Not reported
- UEI
- Not reported
- Solicitation number
- Not reported
- Topic code
- Not reported
Research abstract
DESCRIPTION (provided by applicant): The overall objective of this project is
to establish the scientific rationale for the exogenous administration of a
bicarbonate-buffered and enteric-coated pancrelipase to human immunodeficiency
virus (HIV) positive patients who experience diarrhea due to High Activity
Antiretroviral Therapy (HAART). As a side effect of HAART, many HIV patients
experience mild to severe diarrhea with greasy and oily stool that is similar
to the one experienced by cystic fibrosis (CF) patients. Drug induced diarrhea
causes maldigestion of food, malabsorption of fat-soluble vitamins and
nutrients, reduces the absorption of exogenously administered drugs, and leads
to reduced immunocompetence.
The technical approach for establishing the scientific rationale for the use of
a bicarbonate-buffered and enteric-coated pancrelipase for the treatment of
diarrhea and steatorrhea in HIV positive patients is to demonstrate that the
HAART drugs interfere with any one of the key digestive processes that are
responsible for handling the breakdown of fats and lipids, i.e.,
lipase/colipase and enterokinase catalyzed activation of zymogens to active
enzymes. To achieve this goal the inhibitory effect of HAART drugs on
pancreatic lipase/colipase, proteases and activation of prolipase to active
lipase will be determined by employing specific enzyme assays.
The results of these inhibitory studies will help to elucidate how these
antiretroviral drugs interfere with the digestive activity of pancreatic
lipase/colipase and the zymogen activation cascade that leads to HAART induced
diarrhea and steatorrhea. Furthermore, the information gained from these in
vitro studies will establish the therapeutic rationale for initiating the Phase
II clinical program. The objective of the Phase II program is to demonstrate
the efficacy of the exogenously administered bicarbonate-buffered and
enteric-coated pancrelipase to HIV positive patients for the treatment of
diarrhea due to HAART.
PROPOSED COMMERCIAL APPLICATION: NOT AVAILABLE
Technology keywords
Not reported