New Industry KPIs for Evaluating PHM & VBC IT Vendors Prioritize AI-Driven Insights, Workflow Automation, and Real-World Clinical Impact - Top 2025 Vendors Recognized for Effectiveness and Client Experience
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- This would be Dermata's second patent for DMT410, if issued, using its Spongilla technology to topically deliver botulinum toxin for hyperhidrosis -
- The Company recently entered into a Clinical Trial Collaboration Agreement with Revance to study DMT410 for the treatment of axillary hyperhidrosis -
- The Company also has an issued patent in Japan covering their DMT410 program for the treatment of hyperhidrosis -
Read MoreInitial feasibility study of its soluble, Ph neutral, fast acting granular or powder drug delivery system is complete
Test results support the next development step with Phase 1clinical trial expected to commence in April
Provides Summary of Expected 2025 Milestones
Read MoreThe Department of Justice (DOJ) has announced that it will no longer defend statutory protections that currently shield Administrative Law Judges (ALJs) from removal. This significant shift is expected to bolster MMJ International Holdings' ongoing lawsuit against the Drug Enforcement Administration (DEA), which has been criticized for stalling MMJ's application to cultivate pharmaceutical-grade marijuana for medical research.
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PharmPix further positions itself as a leader in the pharmacy benefit management arena as they are proud to announce their expansion into the Medicare market with the launch of MedArk™, a transformative platform designed to meet the complex needs of Medicare Part D plans.
Read More$165.0 million icotrokinra (formerly JNJ-2113) milestone earned in Q4 2024, received in January 2025
PN-881, a potential best-in-class oral IL-17 receptor antagonist peptide nominated as a development candidate in Q4 2024
Topline results for rusfertide Phase 3 VERIFY clinical trial in polycythemia vera expected in March 2025
Topline results for icotrokinra Phase 2b ANTHEM clinical trial in moderate to severe ulcerative colitis expected in March 2025
Cash, cash equivalents, and marketable securities of $559.2 million as of December 31, 2024, combined with $165.0 million milestone payment, anticipated to provide cash runway through at least end of 2028
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Date: March 31, 2025, 10:36 A.M.
Location: Moderated Poster Theater 7
PROGNOSTIC IMPLICATIONS OF PLATELET FCɣRIIA DURING THE FIRST YEAR AFTER MYOCARDIAL INFARCTION
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With the addition of SBG injections, the West Palm Beach integrative health clinic offers a new option to individuals looking for relief from chronic pain, trauma disorder, and other ailments
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Education event for occupational and environmental medicine physicians will cover biomechanics, research and clinical indications for use of long-duration ultrasound treatment for soft-tissue injury healing.
Read MoreThe closing of the business combination with PowerUp Acquisition Corp. creates Nasdaq-listed biopharmaceutical company dedicated to developing breakthrough innovations in FDA approved drugs, nutraceuticals, and supplements
Aspire has multiple product candidates in key areas of medical needs such as a fast-acting aspirin product for cardiology emergencies and pain management, a proprietary Viagra/Cialis combination product, various bi-hormonal drugs such as testosterone, estrogen, weight loss, anti-seizure, and thyroid drugs. Supplements such as pre-workout and melatonin are already being developed using Aspire's proprietary sublingual delivery system.
Aspire Biopharma Holdings, Inc. ("Aspire Biopharma") is scheduled to begin trading on Nasdaq on February 20, 2025 under the ticker symbol "ASBP".
Read MoreThis study, initiated yesterday, is one of five clinical efforts - three proof-of-concept (POC) investigator-initiated trials (IIT) and two Phase 2 studies - of crofelemer for the rare disease indications of SBS-IF and microvillus inclusion disease (MVID) in the US, EU, and/or Middle East/North Africa regions
Availability of first IIT proof-of-concept results potentially in H1 2025
Crofelemer, Jaguar's novel plant-based prescription drug, has been granted Orphan-Drug Designation by the FDA and the European Medicines Agency (EMA) for both SBS-IF and MVID
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The global leader in dental imaging technologies will showcase the latest innovations added to its digital ecosystem - a suite of tools and software designed to connect the entire digital workflow from diagnosis to delivery.
Read MorePriority Review Vouchers (PRVs) are transferable and, in past transactions by other companies, have sold for prices up to $350 million
1.3 to 4 million cholera cases and 21,000 to 143,000 cholera-related deaths occur each year worldwide
Read MoreThe new study highlights the effectiveness of an automated system in optimizing laboratory test utilization, ensuring medical necessity verification, and streamlining payment processing.
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VIA360™ Surgical System with proprietary ActiveInject™ Technology delivers viscoelastic where you want it, when you want it, giving surgeons unmatched precision and control.
Read MoreFDA-Compliant Clinical Trials:
MMJ's innovative soft gelatin THC-CBD capsule, known as MMJ-002, is undergoing the rigorous FDA approval process to validate the safety and efficacy of cannabis-derived therapeutics for use in human clinical trials for Huntington's disease patients.