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VistaGen Therapeutics

2.36

+0.15006.79%

Post-market: 2.370.0100+0.42%19:41 EDT

Volume:155.57K

Turnover:360.07K

Market Cap:68.11M

PE:-1.53

High:2.38

Open:2.23

Low:2.19

Close:2.21

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Overview Company News Filings

Vistagen Therapeutics Inc expected to post a loss of 51 cents a share - Earnings Preview

Press Release: Vistagen to Report Fiscal Year 2025 Third Quarter Results and Host Corporate Update Conference Call on February 13, 2025

Vistagen granted USPTO patent for AV-101 to treat neuropathic pain

BRIEF-Vistagen Receives U.S. Patent for AV-101 to Treat Neuropathic Pain

Vistagen Receives U.S. Patent for Av-101 to Treat Neuropathic Pain

THOMSON REUTERS

Vistagen Therapeutics Inc - Patent Will Not Expire Until at Least 2034

THOMSON REUTERS

Vistagen Therapeutics-Plans to Seek Potential Strategic Collaborations to Further Advance Potential Clinical Development, Commercialization of Av-101

THOMSON REUTERS

BRIEF-Vistagen Announces Positive Results from Exploratory Phase 2A Study of PH284 in Cancer Cachexia

Vistagen Therapeutics Inc - Phase 2a Study Evaluates Efficacy, Safety, and Tolerability of Ph284

THOMSON REUTERS

Vistagen Announces Positive Results From Exploratory Phase 2a Study of Ph284 in Cancer Cachexia

THOMSON REUTERS

Vistagen Therapeutics Inc - Ph284 Demonstrates No Serious Adverse Events

THOMSON REUTERS

BRIEF-Vistagen Initiates Fasedienol Repeat Dose Study For The Acute Treatment Of Social Anxiety Disorder

Vistagen Initiates Fasedienol Repeat Dose Study for the Acute Treatment of Social Anxiety Disorder

THOMSON REUTERS

Vistagen Initiates Fasedienol Repeat Dose Study for the Acute Treatment of Social Anxiety Disorder

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Phase 2a Study Evaluates Efficacy, Safety, and Tolerability of Ph284","url":"https://stock-news.laohu8.com/highlight/detail?id=2503781785","media":"THOMSON REUTERS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2503781785?lang=en_us&edition=fundamental","pubTime":"2025-01-14 21:30","pubTimestamp":1736861401,"startTime":"0","endTime":"0","summary":null,"market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20250114:nTUABSD0MC:4","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"reuters_en_live","symbols":["VTGN","BK4139"],"gpt_icon":0},{"id":"2503781225","title":"Vistagen Announces Positive Results From Exploratory Phase 2a Study of Ph284 in Cancer Cachexia","url":"https://stock-news.laohu8.com/highlight/detail?id=2503781225","media":"THOMSON REUTERS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2503781225?lang=en_us&edition=fundamental","pubTime":"2025-01-14 21:30","pubTimestamp":1736861401,"startTime":"0","endTime":"0","summary":null,"market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20250114:nTUABSD0MC:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"reuters_en_live","symbols":["BK4139","VTGN"],"gpt_icon":0},{"id":"2503781015","title":"Vistagen Therapeutics Inc - 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Complementing its statistically significant PALISADE-2 U.S. Phase 3 trial of fasedienol for the acute treatment of adults with SAD reported in 2023, Vistagen's U.S. registration-directed PALISADE Phase 3 program for fasedienol for the acute treatment of SAD includes its ongoing PALISADE-3 and PALISADE-4 U.S. Phase 3 trials and a small U.S. Phase 2 repeat dose study. PALISADE-3 and PALISADE-4 are each a multi-center randomized, double-blind, placebo-controlled Phase 3 trial designed similarly to PALISADE-2 to evaluate the efficacy, safety, and tolerability of the acute administration of fasedienol to relieve anxiety symptoms in subjects with SAD induced by a public speaking challenge conducted in a clinical setting. Vistagen believes either PALISADE-3 or PALISADE-4, if successful, together with PALISADE-2, may establish substantial 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