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AIM ImmunoTech Announces Positive Safety Data in First Cohort of Phase 1 Clinical Study

Press release content from Globe Newswire. The AP news staff was not involved in its creation. AIM ImmunoTech Announces Positive Safety Data in First Cohort of Phase 1 Clinical Study . AIM ImmunoTech Inc.April 7, 2021 GMT OCALA, Fla., April 07, 2021 (GLOBE NEWSWIRE) AIM ImmunoTech Inc. (NYSE American: AIM) today announced that it has completed dosing of Cohort 1 in a Phase 1 clinical study on the safety of AIM’s drug Ampligen as an intranasal therapy, reporting no serious adverse events, and paving the way for escalation of the dose in Cohort 2. The trial is a critical step in the company’s ongoing efforts to develop Ampligen as a potential prophylaxis or treatment for COVID-19 and other respiratory viral diseases.

United statesThomask equelsCentre for human drug researchImmunotech incCrescendo communicationsHuman drug researchPlacebo controlled studyRepeated intranasal administrationHealthy subjectsPrivate securities litigation reform actTech incஒன்றுபட்டது மாநிலங்களில்மையம் க்கு மனிதன் மருந்து ஆராய்ச்சிபிறை தகவல்தொடர்புகள்மனிதன் மருந்து ஆராய்ச்சிமருந்துப்போலி கட்டுப்படுத்தப்படுகிறது படிப்பு

AIM ImmunoTech Inc : AIM ImmunoTech Announces Positive Safety Data in First Cohort of Phase 1 Clinical Study Investigating Intranasal Administration of Ampligen as a Potential Prophylaxis or Treatment for COVID-19 and Other Respiratory Viral Diseases

AIM ImmunoTech Inc : AIM ImmunoTech Announces Positive Safety Data in First Cohort of Phase 1 Clinical Study Investigating Intranasal Administration of Ampligen as a Potential Prophylaxis or Treatment for COVID-19 and Other Respiratory Viral Diseases
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United statesThomask equelsCentre for human drug researchImmunotech incCrescendo communicationsHuman drug researchPlacebo controlled studyRepeated intranasal administrationHealthy subjectsPrivate securities litigation reform actஒன்றுபட்டது மாநிலங்களில்மையம் க்கு மனிதன் மருந்து ஆராய்ச்சிபிறை தகவல்தொடர்புகள்மனிதன் மருந்து ஆராய்ச்சிமருந்துப்போலி கட்டுப்படுத்தப்படுகிறது படிப்புஆரோக்கியமான பாடங்கள்

New England Journal of Medicine Publishes 24-Week Results from Phase 3 Study Evaluating RINVOQ in Psoriatic Arthritis

ABBVie today announced that the New England Journal of Medicine has published 24-week results from the Phase 3 SELECT-PsA 1 trial evaluating RINVOQ ™ in adults with active psoriatic arthritis who had responded inadequately or were intolerant to one or more non-biologic disease modifying anti-rheumatic drugs . 1 These data build on previously announced Phase 3 topline results showing that upadacitinib 15 mg and 30 … ABBVie (NYSE: ABBV) today announced that the New England Journal of Medicine has published 24-week results from the Phase 3 SELECT-PsA 1 trial evaluating RINVOQ ™ (upadacitinib, 15 mg and 30 mg) in adults with active psoriatic arthritis who had responded inadequately or were intolerant to one or more non-biologic disease modifying anti-rheumatic drugs (DMARDs). 1 These data build on previously announced Phase 3 topline results showing that upadacitinib 15 mg and 30 mg met the primary endpoint of ACR20 response at week 12 versus placebo as well as key secondary endpo

United statesUnited kingdomThomas hudsonIain mcinnesExchange commissionAbbvie incEuropean commissionNew england journalLeeds enthesitis indexInvestigator global assessmentHeijde scoreLeeds dactylitis indexVersus arthritis professorFunctional assessmentChronic illness therapy fatigueImportant safety information

New England Journal of Medicine Publishes 24-Week Results from Phase 3 Study Evaluating RINVOQ™ (upadacitinib) in Psoriatic Arthritis

Share this article NORTH CHICAGO, Ill., April 1, 2021 /PRNewswire/ AbbVie (NYSE: ABBV) today announced that the New England Journal of Medicine has published 24-week results from the Phase 3 SELECT-PsA 1 trial evaluating RINVOQ ™ (upadacitinib, 15 mg and 30 mg) in adults with active psoriatic arthritis who had responded inadequately or were intolerant to one or more non-biologic disease modifying anti-rheumatic drugs (DMARDs). 1 These data build on previously announced Phase 3 topline results showing that upadacitinib 15 mg and 30 mg met the primary endpoint of ACR20 response at week 12 versus placebo as well as key secondary endpoints. 1 These data show upadacitinib s potential to improve clinical and radiographic outcomes for people with psoriatic arthritis, a complex and progressive autoimmune disease, said Thomas Hudson, MD, senior vice president, research and development, chief scientific officer, AbbVie. Ultimately, our goal is to help more patients achieve d

United statesUnited kingdomThomas hudsonIain mcinnesEuropean commissionExchange commissionAbbvie incNew england journalLeeds enthesitis indexVersus arthritis professorInvestigator global assessmentHeijde scoreFunctional assessmentChronic illness therapy fatigueImportant safetyMississippi river

Adamis Pharmaceuticals Announces Tempol Reduces Lung Inflammation in the COVID-19 Challenged Hamster Model

Share: SAN DIEGO, March 15, 2021 (GLOBE NEWSWIRE) Adamis Pharmaceuticals Corporation (NASDAQ:ADMP) ( Company ) announced today that in studies conducted at Galveston National Laboratory (GNL), University of Texas Medical Branch (UTMB) at Galveston, hamsters challenged with the virus that causes COVID-19 (SARS-CoV-2), resulted in decreased inflammation in the lungs of animals treated with Tempol compared to controls. This is the first data demonstrating that Tempol, a novel antioxidant, can reduce inflammation in animals given the virus (SARS-CoV-2) that causes COVID-19. The group plans on submitting the publication to a peer review journal. Dr. Chien-Te Kent Tseng, Professor of the Department of Microbiology and Immunology and Director of GNL s SARS/MERS/COVID-19 Laboratory at UTMB, commented on these results: In our hamster COVID-19 model, pulmonary inflammation with cellular infiltrates and hemorrhage (mild-to-moderate) is triggered by SARS-CoV-2 infection. Treatment with T

United statesAleksandrak drelichRonald mossDennisj carloKempaiah rayavaraMark flatherKent tsengAdamis pharmaceuticals corporationCompounding incAdamis pharmaceuticalsUniversity of texas medical branchGalveston national laboratoryCorporate communicationsProfessor of the department microbiologyStanford universityPharmaceuticals corporation