Akari Therapeutics Receives FDA Feedback, Paving the Way for New Eye Disease Treatment
Portfolio Pulse from Benzinga Newsdesk
Akari Therapeutics received positive Pre-IND feedback from the FDA for its eye disease treatment, PAS-nomacopan. This feedback clarifies the company's preclinical plans, drug manufacturing, and Phase 1 clinical strategy. The IND is expected to be submitted in 2025.
August 19, 2024 | 12:02 pm
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Akari Therapeutics received positive FDA feedback for its eye disease treatment, PAS-nomacopan. This feedback clarifies the company's preclinical plans, drug manufacturing, and Phase 1 clinical strategy. The IND is expected to be submitted in 2025.
The positive FDA feedback is a significant regulatory milestone for Akari Therapeutics, providing a clear path forward for its eye disease treatment. This is likely to boost investor confidence and positively impact the stock price in the short term.
CONFIDENCE 90
IMPORTANCE 80
RELEVANCE 100