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Moleculin Biotech

0.8201

-0.0486-5.60%

Post-market: 0.8001-0.0199-2.43%19:50 EDT

Volume:487.21K

Turnover:393.17K

Market Cap:11.48M

PE:-0.07

High:0.8467

Open:0.8467

Low:0.7600

Close:0.8687

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Overview Company News Filings

Why Is Blood Cancer Focused Moleculin Biotech Stock Trading More Than 400% On Thursday?

Moleculin Announces Exercise of Warrants for $5.8 Million Gross Proceeds

Moleculin Biotech Gets FDA Nod for Phase 3 Trial

BRIEF-Moleculin Receives Positive FDA Guidance For Its Trial For R/R Acute Myeloid Leukemia

Moleculin Biotech Inc - FDA Allows Reduction in Size of Moleculin's Phase 3 Trial

THOMSON REUTERS

Moleculin Receives Positive FDA Guidance for Acceleration of Its Registration-Enabling Miracle Trial for R/R Acute Myeloid Leukemia (Aml)

THOMSON REUTERS

Moleculin Biotech Inc - Amended Protocol Allows Unblinding of Data at 45 Subjects

THOMSON REUTERS

Moleculin Biotech Inc - First Unblinding Expected in Second Half of 2025

THOMSON REUTERS

Moleculin Biotech Inc : Maxim Group Cuts to Hold From Buy

THOMSON REUTERS

Moleculin Biotech downgraded to Hold from Buy at Maxim

Moleculin Biotech Receives Approval in Ukraine to Start Recruiting for Acute Myeloid Leukemia Phase 3 Trial

MT Newswires Live

Moleculin Biotech Gains European Approval for Phase 3 Trial

BRIEF-Moleculin Receives First Country Approval In Europe To Begin Recruiting For Phase 3 R/R Acute Myeloid Leukemia Trial

Moleculin Biotech receives first approval in Europe for AML trial recruiting

Moleculin Receives First Country Approval in Europe to Begin Recruiting for the Miracle Phase 3 R/R Acute Myeloid Leukemia (Aml) Pivotal Trial

THOMSON REUTERS

Moleculin Biotech Inc - First Subject Treatment in Miracle Trial Expected Q1 2025

THOMSON REUTERS

Moleculin Biotech Launches MIRACLE Study for AML

Moleculin Biotech (MBRX) Gets a Buy from Roth MKM

Moleculin Highlights Development Progress of Annamycin, Phase 2 Data Outperforms Billion-Dollar Assets in Aml, Phase 3 Data Readouts in 2025 & 2026

THOMSON REUTERS

Moleculin Biotech: on Track to Begin Dosing of Annamycin in Combination With Cytarabine for Treatment of R/R Aml in Q1 2025

THOMSON REUTERS

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Moreover, the nature of the feedback helps us move forward quickly to open sites in the US, in addition to the sites we are expecting to open inEuropeand theMiddle East. All of this supports the pursuit of an accelerated timeline for new drug approval,” commentedWalter Klemp, Chairman and Chief Executive Officer of Moleculin.The MIRACLE Phase 3 study utilizes an adaptive design whereby the first 75 to 90 subjects will be randomized in Part A of the trial to receive high-dose cytarabine  combined with either placebo, 190 mg/m2 of Annamycin, or 230 mg/m2 of Annamycin, which Annamycin doses were recommen","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://finance.yahoo.com/news/why-blood-cancer-focused-moleculin-181902418.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["MBRX","BK4139"],"gpt_icon":0},{"id":"2511576810","title":"Moleculin Announces Exercise of Warrants for $5.8 Million Gross Proceeds","url":"https://stock-news.laohu8.com/highlight/detail?id=2511576810","media":"PR Newswire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2511576810?lang=en_us&edition=fundamental","pubTime":"2025-02-14 02:05","pubTimestamp":1739469900,"startTime":"0","endTime":"0","summary":"HOUSTON, Feb. 13, 2025 /PRNewswire/ -- Moleculin Biotech, Inc.,  , a late-stage pharmaceutical company with a broad portfolio of drug candidates targeting hard-to-treat tumors and viruses, today announced it has entered into agreements with certain holders of its existing warrants for the immediate exercise of certain outstanding warrants to purchase up to an aggregate of 5,828,570 shares of common stock of the Company originally issued in December 2023 and August 2024 all at a reduced exercise price of $1.00 per share. The shares of common stock issuable upon exercise of the outstanding warrants are registered pursuant to effective registration statements on Form S-1  and on Form S-1 . 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Published first on TheFly – the ultimate source for real-time, market-moving breaking f...","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/the-fly/moleculin-biotech-downgraded-to-hold-from-buy-at-maxim?utm_source=itigerup.com&utm_medium=referral","rn_cache_url":null,"directOrigin":true},"property":["rate"],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.tipranks.com/news/the-fly/moleculin-biotech-downgraded-to-hold-from-buy-at-maxim?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":["MBRX"],"gpt_icon":0},{"id":"2510331120","title":"Moleculin Biotech Receives Approval in Ukraine to Start Recruiting for Acute Myeloid Leukemia Phase 3 Trial","url":"https://stock-news.laohu8.com/highlight/detail?id=2510331120","media":"MT Newswires Live","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2510331120?lang=en_us&edition=fundamental","pubTime":"2025-02-12 00:18","pubTimestamp":1739290714,"startTime":"0","endTime":"0","summary":"Moleculin Biotech  said Tuesday it received regulatory approval in Ukraine to start recruiting for a phase 3 trial of annamycin plus cytarabine to treat relapsed or refractory acute myeloid leukemia, a type of cancer.The first 75 to 90 subjects in the trial's part A will receive high-dose cytarabine, or HiDAC, combined with either placebo or various doses of annamycin, the company said.For part B, roughly 244 additional subjects will receive either HiDAC plus placebo or HiDAC plus the optimum dose of annamycin, up from 240 subjects. Moleculin said the increase in the number of subjects represents the \"statistical 'cost' of the additional interim unblinding.\"Moleculin Biotech said it remains on track to treat a first subject in the phase 3 trial in Q1.Shares were down over 16% in recent trading.Price: 0.59, Change: -0.12, Percent Change: -16.34","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://www.mtnewswires.com/","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":"mtnewswires_news","symbols":["MBRX","BK4139"],"gpt_icon":0},{"id":"2510380257","title":"Moleculin Biotech Gains European Approval for Phase 3 Trial","url":"https://stock-news.laohu8.com/highlight/detail?id=2510380257","media":"TIPRANKS","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2510380257?lang=en_us&edition=fundamental","pubTime":"2025-02-11 22:48","pubTimestamp":1739285323,"startTime":"0","endTime":"0","summary":"The latest update is out from Moleculin Biotech ( ($MBRX) ). 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