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News · 26 weeks113+10%
2025-10-262026-04-19
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Latest news
25 items- SECSEC Form 424B3 filed by Medicus Pharma Ltd.424B3 - Medicus Pharma Ltd. (0001997296) (Filer)
- SECSEC Form PRE 14A filed by Medicus Pharma Ltd.PRE 14A - Medicus Pharma Ltd. (0001997296) (Filer)
- PRMedicus Pharma Submits Orphan Drug Designation Application to U.S. FDA for SkinJect® in Gorlin SyndromePHILADELPHIA, April 17, 2026 (GLOBE NEWSWIRE) -- Medicus Pharma Ltd. (NASDAQ:MDCX) ("Medicus" or the "Company"), a biotech/life sciences company focused on advancing the clinical development programs of novel and potentially disruptive therapeutics assets, today announced the submission of an Orphan Drug Designation (ODD) application to the U.S. Food and Drug Administration for SkinJect® (D-MNA) for the treatment of basal cell carcinoma (BCC) in patients with Gorlin Syndrome, a rare genetic disorder characterized by the development of multiple, recurrent skin cancers. The submission represents a strategic expansion of the SkinJect program into a high unmet need orphan indication, where cu
- PRMedicus Pharma to Present New Teverelix Data at AACE 2026 Demonstrating Long-Acting Hormone SuppressionPHILADELPHIA, April 15, 2026 (GLOBE NEWSWIRE) -- Medicus Pharma Ltd. (NASDAQ:MDCX) ("Medicus" or the "Company"), a biotech/life sciences company focused on advancing the clinical development programs of novel and potentially disruptive therapeutics assets, today announced it will present new Phase 1 clinical data on Teverelix, its investigational long-acting gonadotropin-releasing hormone (GnRH) antagonist, at the American Association of Clinical Endocrinology Annual Meeting 2026 (AACE 2026) on April 22-24th in Las Vegas, Nevada. Teverelix is being developed for hormone-driven conditions, with potential applications in women's health, including endometriosis and uterine fibroids. Faisal
- PRMedicus Pharma Submits Optimized Phase 2 Study Protocol to U.S. FDA for Teverelix in Acute Urinary RetentionPHILADELPHIA, April 06, 2026 (GLOBE NEWSWIRE) -- Medicus Pharma Ltd. (NASDAQ:MDCX) ("Medicus" or the "Company"), a biotech/life sciences company focused on advancing the clinical development programs of novel and potentially disruptive therapeutics assets, today announced the Company has submitted an optimized Phase 2 clinical study design to the U.S. Food and Drug Administration ("FDA") for Teverelix, its investigational GnRH antagonist, for the prevention of recurrent acute urinary retention ("AURr") in men with benign prostatic hyperplasia ("BPH") as part of its existing open Investigational New Drug ("IND") for Teverelix. The Phase 2 study design has been refined under the leadership
- INSIDERSEC Form 4 filed by Smith Andrew Alasdair4 - Medicus Pharma Ltd. (0001997296) (Issuer)
- INSIDERSEC Form 4 filed by Rodgers Cathy Mcmorris4 - Medicus Pharma Ltd. (0001997296) (Issuer)
- INSIDERSEC Form 4 filed by Raju Ajay4 - Medicus Pharma Ltd. (0001997296) (Issuer)
- INSIDERSEC Form 4 filed by Mehmud Faisal4 - Medicus Pharma Ltd. (0001997296) (Issuer)
- INSIDERSEC Form 4 filed by May Sara R.4 - Medicus Pharma Ltd. (0001997296) (Issuer)
- INSIDERSEC Form 4 filed by Mahaffy Patrick J4 - Medicus Pharma Ltd. (0001997296) (Issuer)
- INSIDERSEC Form 4 filed by Kaiser Larry4 - Medicus Pharma Ltd. (0001997296) (Issuer)
- INSIDERSEC Form 4 filed by Fishman Barry4 - Medicus Pharma Ltd. (0001997296) (Issuer)
- INSIDERSEC Form 4 filed by Ciaruffoli Robert J.4 - Medicus Pharma Ltd. (0001997296) (Issuer)
- INSIDERSEC Form 4 filed by Brennan Edward J.4 - Medicus Pharma Ltd. (0001997296) (Issuer)
- INSIDERSEC Form 4 filed by Bonner Carolyn F.4 - Medicus Pharma Ltd. (0001997296) (Issuer)
- INSIDERSEC Form 4 filed by Bokhari Raza4 - Medicus Pharma Ltd. (0001997296) (Issuer)
- INSIDERSEC Form 4 filed by Ashton William4 - Medicus Pharma Ltd. (0001997296) (Issuer)
- PRMedicus Pharma Ltd Clarifies Positive SkinJect Phase 2 DatasetPHILADELPHIA, April 01, 2026 (GLOBE NEWSWIRE) -- Medicus Pharma Ltd. (NASDAQ:MDCX) ("Medicus" or the "Company"), a biotech/life sciences company focused on advancing the clinical development programs of novel and potentially disruptive therapeutics assets, today issued a clarification regarding previously reported topline results from its Phase 2 clinical study of SKNJCT-003 in nodular basal cell carcinoma (BCC). SkinJect, an investigational doxorubicin-containing microneedle array (D-MNA), is being developed as a potential non-surgical treatment option for patients with nodular BCC, a common form of skin cancer currently treated primarily with surgical intervention. If confirmed in futu
- PRMedicus Pharma Reports KOL Validation of SkinJect Phase 2 Data of 80% Overall Response RatePHILADELPHIA, March 30, 2026 (GLOBE NEWSWIRE) -- Medicus Pharma Ltd. (NASDAQ:MDCX) ("Medicus" or the "Company"), a biotech/life sciences company focused on advancing the clinical development programs of novel and potentially disruptive therapeutics assets, today reported independent clinical validation of its Phase 2 SkinJect® dataset from Dr. Babar Rao, principal investigator of the SKNJCT-003 study and a globally recognized dermatology key opinion leader. Dr. Rao's independent assessment reinforces the Company's view that the dataset is clinically meaningful, decision-grade, and supportive of continued development and regulatory engagement. Dr. Rao, speaking in his capacity as princip
- SECSEC Form EFFECT filed by Medicus Pharma Ltd.EFFECT - Medicus Pharma Ltd. (0001997296) (Filer)
- SECSEC Form EFFECT filed by Medicus Pharma Ltd.EFFECT - Medicus Pharma Ltd. (0001997296) (Filer)
- SECSEC Form EFFECT filed by Medicus Pharma Ltd.EFFECT - Medicus Pharma Ltd. (0001997296) (Filer)
- PRMedicus Pharma Business Update Call to Highlight 80% Overall Response Rate (ORR) in Phase 2 SkinJect Study and Agentic AI-enabled Drug Development PlanPHILADELPHIA, March 26, 2026 (GLOBE NEWSWIRE) -- Medicus Pharma Ltd. (NASDAQ:MDCX) ("Medicus" or the "Company"), a biotech/life sciences company focused on advancing the clinical development programs of novel and potentially disruptive therapeutics assets, today announced it will host a business update conference call at 11:30 a.m. Eastern Time. The call will highlight new analysis from its Phase 2 SkinJect® study, including an overall response rate (ORR) of 80% in the 200µg cohort at Day 57, and outline the Company's planning toward an agentic AI–enabled clinical development platform. The Company believes these results position the 200µg cohort as the leading dose regimen in the study,
- SECSEC Form POS AM filed by Medicus Pharma Ltd.POS AM - Medicus Pharma Ltd. (0001997296) (Filer)