- Dermata expects to announce topline results from its XYNGARI™ Phase 3 Spongilla Treatment of Acne Research (STAR-1) clinical trial by end of March 2025 -
- The Company recently entered into a Clinical Trial Collaboration Agreement with Revance Therapeutics (recently merged with Crown Laboratories) to study DMT410 for the treatment of axillary hyperhidrosis -
- Raised $2.55 million in gross proceeds from a private placement financing in January 2025, including participation from Dermata's Chief Executive Officer, Chief Financial Officer, and certain members of the Company's board of directors -
The creators of the sam® sustained acoustic medicine technology present its proven ability to speed recovery and soft tissue healing at the University of Louisiana basketball game, part of the company's commitment to helping athletes stay healthy.
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MedSmart Wellness Centers Inc. Signs Letter of Intent to Acquire 3,000 Sq. Ft. Facility in Tequesta, Florida
Read MoreMonogram May Market the Monogram mBôs™ TKA System, Subject to the Requirements of the Federal Food, Drug, and Cosmetic Act (the Act).
The Company is Preparing for Commercialization and Evaluating Strategies to Support the Adoption of its Robotic-Assisted Technology
Read MoreJaguar expects first results in Q2 2025 of proof-of-concept investigator-initiated trials of crofelemer for the rare diseases short bowel syndrome with intestinal failure and microvillus inclusion disease
FDA meeting expected in Q2 2025 on the statistically significant results of the Phase 3 OnTarget trial of crofelemer in the prespecified subgroup of patients with breast cancer
Read MoreAnother key win in expanding AI Nose's industrial opportunities
Partnership to integrate AI Nose into ASE's factories and explore broader industrial use-cases
Read MoreInstallation Coincides with Previously Announced TRNR Presence at HFA 2025, Adds to Growing US & International Presence of Fast-Growing Company
Mandalay Bay Resort Fitness Center Reportedly One of Most-Visited Gyms in US
Read MoreThis Press Release is Acting as a Correction to the Financial Tables in the Previous Release
Completed all Supplemental Testing and has Submitted its Formal Response to the FDA's Additional Information Request (AIR)
Management to Host Business Update Conference Call on Wednesday, March 12, 2025, at 4:30 p.m. Eastern Time
Read MoreCompleted all Supplemental Testing and has Submitted its Formal Response to the FDA's Additional Information Request (AIR)
Management to Host Business Update Conference Call on Wednesday, March 12, 2025, at 4:30 p.m. Eastern Time
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This post was written and published as a collaboration between the in-house editorial team at Benzinga and Tonix Pharmaceuticals Holding Corp. with financial support from Tonix. The two organizations work to ensure that any and all information contained within is true and accurate as of the date hereof to the best of their knowledge and research. This content is for informational purposes only and not intended to be investing advice.
Read MoreLatest investment follows previously-announced investment in TRNR of $2.9M, reflecting investor's increased enthusiasm for Company's growth and acquisition strategy, including last week's Letter of Intent
Company looks forward to appearing at this week's HFA Summit in Las Vegas
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As the automotive and electronics industries undergo rapid transformation, HAHN Automation Group is setting new benchmarks in technological excellence. With over 30 years of experience, a strong U.S. presence, and a global network, we are uniquely positioned to address industry challenges and drive automation forward.
Read MoreClinical response rate of 63.5% and clinical remission rate of 30.2% achieved at Week 12 with the highest dose, which continued to improve through Week 28
All three doses met the primary endpoint of clinical response at Week 12, with a favorable safety profile
These results in ulcerative colitis build on strong data recently reported for the plaque psoriasis Phase 3 program
Read MoreNearly half of patients with moderate-to-severe plaque psoriasis (PsO) treated with icotrokinra achieved completely clear skin (IGA 0) at Week 24 in Phase 3 ICONIC-LEAD study
Topline results from Phase 3 ICONIC-ADVANCE 1&2studies show icotrokinra achieved co-primary endpoints and showed superiority to deucravacitinib in moderate-to-severe PsO
Results pave the way to initiate the first-ever head-to-head study (ICONIC-ASCEND) seeking to demonstrate the superiority of a pill versus injectable biologic in moderate-to-severe PsO
Read MoreUnveiled revolutionary AI Nose for robotics application, inviting global robotics companies to join Ainos Alliance in shaping the future of smell-enabled robots
Advanced VELDONA® development with key Japan patent, Taiwan Tanabe partnership, and IRB approval for Sjögren's syndrome clinical study
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