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Inhibikase Therapeutics, Inc.

2.50

+0.11004.60%

Post-market: 2.530.0280+1.12%19:51 EDT

Volume:735.93K

Turnover:1.83M

Market Cap:350.00M

PE:-5.78

High:2.54

Open:2.41

Low:2.35

Close:2.39

52wk High:2.54

52wk Low:1.33

Shares:140.00M

Float Shares:64.52M

Volume Ratio:1.58

T/O Rate:1.14%

Dividend:- -

Dividend Rate:- -

EPS(TTM):-0.4327

EPS(LYR):-0.4909

ROE:-51.96%

ROA:-32.79%

PB:2.28

PE(LYR):-5.09

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Overview Company News Filings

Inhibikase Shareholders Approve Governance and Compensation Changes

Inhibikase Therapeutics Holds Annual Shareholder Meeting

Inhibikase Therapeutics Inc : Oppenheimer Initiates Coverage With Outperform Rating and Target Price $5

THOMSON REUTERS

Inhibikase Therapeutics initiated with an Outperform at Oppenheimer

Oppenheimer Initiates Inhibikase Therapeutics at Outperform

MT Newswires Live

Inhibikase Therapeutics: Buy Rating Reiterated on Advancing Phase 3 PAH Program and Robust IP, Price Target Maintained at $8

LifeSci Capital Keeps Their Buy Rating on Inhibikase Therapeutics (IKT)

Analysts Are Bullish on These Healthcare Stocks: Milestone Scientific (MLSS), Inhibikase Therapeutics (IKT)

Inhibikase Therapeutics Inc reports results for the quarter ended March 31 - Earnings Summary

Inhibikase Therapeutics Q1 EPS $(0.10) Beats $(0.13) Estimate

Benzinga Earnings

Inhibikase Therapeutics Announces First Quarter 2026 Financial Results and Highlights Recent Activity

THOMSON REUTERS

Inhibikase Advances IKT-001 Into Adaptive Phase 3 Trial for Pulmonary Arterial Hypertension

Inhibikase Therapeutics Inc expected to post a loss of 11 cents a share - Earnings Preview

Inhibikase Therapeutics announces annual shareholder meeting webcast

Buy Rating on IKT-001: De-Risked Late-Stage PAH Program with Adaptive Phase 3 Design and Solid Financial Runway

Inhibikase Therapeutics: Phase 3 IKT-001 PAH Program and De-Risked Imatinib-Based Efficacy Drive Buy Rating and $8 Target

Inhibikase Begins Pivotal Phase 3 Trial in PAH

Inhibikase enrolls first patient in Phase 3 IMPROVE-PAH trial for IKT-001

Inhibikase Therapeutics Announces Enrollment of First Patient in Improve-Pah Global Phase 3 Study of Ikt-001 in the Treatment of Pulmonary Arterial Hypertension

THOMSON REUTERS

Inhibikase grants 685,718 inducement stock options to five new hires at $1.68/share

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On April 7, 2026, Inhibikase Therapeutics announced it had enrolled the f...","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/company-announcements/inhibikase-begins-pivotal-phase-3-trial-in-pah?utm_source=itigerup.com&utm_medium=referral","rn_cache_url":null,"directOrigin":true},"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.tipranks.com/news/company-announcements/inhibikase-begins-pivotal-phase-3-trial-in-pah?utm_source=itigerup.com&utm_medium=referral","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"tipranks_highlight","symbols":["IKT","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2625893013","title":"Inhibikase enrolls first patient in Phase 3 IMPROVE-PAH trial for IKT-001","url":"https://stock-news.laohu8.com/highlight/detail?id=2625893013","media":"Reuters","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2625893013?lang=en_us&edition=fundamental","pubTime":"2026-04-07 20:06","pubTimestamp":1775563569,"startTime":"0","endTime":"0","summary":"Inhibikase Therapeutics enrolled first patient in IMPROVE-PAH, a global Phase 3 study of oral PAH candidate IKT-001.Results have not been presented; trial is designed to generate pivotal data to support a potential NDA filing.Study will assess whether IKT-001 can improve pulmonary blood flow function, physical capacity, and disease progression measures versus placebo.Program positions IKT-001 as a reformulated approach to imatinib intended to reduce gastrointestinal side effects seen with the older drug.Trial is planned for up to 180 sites worldwide, using an adaptive design with two sequential parts covering about 486 patients.Disclaimer: This news brief was created by Public Technologies  using generative artificial intelligence. 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