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Lonza Group AG: NextPharma Set to Acquire Two Lonza Sites Specialized in Lipid Oral Dosage Forms

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NextPharma Set to Acquire Two Lonza Sites Specialized in Lipid Oral Dosage Forms
Agreement initiates process for future acquisition of Lonza sites in Ploermel (FR) and Edinburgh (UK) allowing NextPharma to broaden technology offering into lipid finished dosage forms
Centers of excellence employing a total of 390 staff offer expertise in Lipid Oral Dosage Forms including softgels and liquid-filled hard capsules for the pharma and nutrition markets
Sustainable growth and people development a priority for both companies
A French version of this release is also available
Quote from Gordon Bates, President and Head of Small Molecules, Lonza:
NextPharma is an established and well-respected company, with extensive experience in oral and topical finished dosage forms. As such, it is the ideal buyer given the technologies available at the Ploermel and Edinburgh sites. We are confident that the capabilities and experience at the two sites are a complementar ....

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U.S. Stem Cell, Inc.: USRM Oral Argument in Appeal from FDA Enforcement Action

U.S. Stem Cell, Inc.: USRM Oral Argument in Appeal from FDA Enforcement Action
SUNRISE, FL / ACCESSWIRE / January 19, 2021 / U.S. Stem Cell, Inc. (OTC PINK:USRM), a leader in the development of proprietary, physician-based, and novel regenerative medicine solutions, is pleased to announce that oral arguments in the case United States v. U.S. Stem Cell Clinic, LLC, et al., took place on January 13, 2021, before the federal Eleventh Circuit Court of Appeals. The oral argument was held on the Company s appeal of a judgment denying it the right to present evidence and testimony in support of its position and practices in a trial. The Company continues to maintain it should be afforded the opportunity to support its position in such a trial. ....

United States , Mike Tomas , Exchange Commission , Eleventh Circuit Court , Us Stem Cell Inc , Us Stem Cell Clinic , Drug Administration , Us Department Of Justice , Cell Clinic , Cosmetic Act , Southern District , Hcell Inc , Looking Statements , Corporate Parkway , ஒன்றுபட்டது மாநிலங்களில் , மைக் டோமாக்கள் , பரிமாற்றம் தரகு , பதினொன்றாவது சுற்று நீதிமன்றம் , எங்களுக்கு தண்டு செல் இன்க் , எங்களுக்கு தண்டு செல் சிகிச்சையகம் , எங்களுக்கு துறை ஆஃப் நீதி , செல் சிகிச்சையகம் , ஒப்பனை நாடகம் , தெற்கு மாவட்டம் , செல் இன்க் , பார்க்கிறது அறிக்கைகள் ,

Key Capital Corporation: Key Capital COVID-19 Oral Pill Vaccine Records 90% Reduction in Virus Infectivity in Early Study

Key Capital Corporation: Key Capital COVID-19 Oral Pill Vaccine Records 90% Reduction in Virus Infectivity in Early Study
NEW YORK, NY / ACCESSWIRE / January 18, 2021 / KEY CAPITAL CORPORATION (OTC PINK:KCPC)
is pleased to
advise that current independent laboratory testing of its partnered Immunitor COVID-19 patented oral pill vaccine in an ongoing university study is providing promising early support for safety and efficacy of the vaccine.
The preliminary tests conducted by a leading Asian research institute have shown safety and a 90% reduction on virus infectivity in mammalian cells following exposure to the active vaccine. This laboratory testing highlights the vaccine methodology and ability to inactivate and/or prevent viral infection and its potential for oral mucosal administration. ....

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Knopp Biosciences LLC: Knopp Biosciences Announces Positive Top-Line Results from the Phase 2 EXHALE Trial of Oral Dexpramipexole in Moderate-to-Severe Eosinophilic Asthma

Knopp Biosciences LLC: Knopp Biosciences Announces Positive Top-Line Results from the Phase 2 EXHALE Trial of Oral Dexpramipexole in Moderate-to-Severe Eosinophilic Asthma
Reduction in blood eosinophil count correlated with clinically important improvement in lung function
Knopp Biosciences LLC today announced positive top-line results in a Phase 2 dose-ranging trial of the novel oral drug dexpramipexole in patients with moderate-to-severe eosinophilic asthma.
The EXHALE study met its primary endpoint, with dexpramipexole demonstrating a statistically significant, dose-dependent reduction in blood absolute eosinophil count (AEC) from Baseline to Week 12 compared to placebo when added to standard of care. The magnitude of change in blood AEC was consistent with the eosinophil depletion seen in previous clinical trials of dexpramipexole in other indications. ....

Michael Bozik , Kostenloser Wertpapierhandel , Tom Petzinger , Knopp Biosciences , Drug Administration , Make Treatment Decisions , மைக்கேல் போசிக் , டோம் பெட்ஸிங்கர் , க்னொபப் உயிர் அறிவியல் , செய்ய சிகிச்சை முடிவுகள் , மூச்சை வெளியேற்றவும் ,

FDA Conditionally Approves First Oral Tablet Laverdia-CA1 To Treat Dogs With Lymphoma

WASHINGTON (dpa-AFX) - The U.S. Food and Drug Administration has conditionally approved first oral tablet Laverdia-CA1 to treat dogs with lymphoma.Lymphoma is a type of cancer of the lymph nodes ....

United States , Kostenloser Wertpapierhandel , Drug Administration , ஒன்றுபட்டது மாநிலங்களில் ,