June 3 (Reuters) - NanoViricides Inc NNVC.A :
* NANOVIRICIDES HAS RECEIVED FAVORABLE FDA COMMENTS ON ITS
PRE-IND
APPLICATION FOR THE LEAD DRUG CANDIDATE
* NANOVIRICIDES - U.S. FDA GENERALLY AGREED IN ITS PRE-IND
RESPONSE THAT PLAN OF DRUG DEVELOPMENT PRESENTED BY CO TO FDA IS
GENERALLY ADEQUATE AT THIS TIME
* NANOVIRICIDES INC - U.S. FDA HAS AGREED THAT COMPANY'S
STRATEGY
FOR DRUG SUBSTANCE AND DRUG PRODUCT ACCEPTANCE CRITERIA IS
ADEQUATE
* NANOVIRICIDES INC - ADDITIONAL NON-CLINICAL STUDIES
RECOMMENDED
BY AGENCY ARE GENERALLY CONSISTENT WITH CO'S PLANNED
IND-ENABLING NON-CLINICAL STUDIES
* NANOVIRICIDES - PROCEEDING WITH COMPLETING IND-ENABLING
STUDIES,
WORKING TO ENGAGE APPROPRIATE CLINICAL STUDY SITES & DEVELOPING
CONCRETE CLINICAL STUDY PLANS
Source text for Eikon: ID:nPn5MhHrJa
Further company coverage: NNVC.A
((Reuters.Briefs@thomsonreuters.com;))