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AIM ImmunoTech Inc reports positive safety data in Cohort 2 of Phase 1 clinical study of Ampligen as an intranasal therapy

AIM ImmunoTech reports positive safety data in Cohort 2 of Phase 1 clinical study of Ampligen as an intranasal therapy The clinical study is crucial for the company s ongoing efforts to develop Ampligen as a potential prophylaxis or treatment for coronavirus (COVID-19) and other respiratory viral diseases AIM ImmunoTech, which also reported no serious adverse events in Cohort 1, said the study will proceed with enrollment into Cohort 3 AIM ImmunoTech Inc (NYSEAMERICAN:AIM) said it has completed dosing of Cohort 2 in a Phase 1 clinical study to assess the safety, tolerability, and biological activity of Ampligen as an intranasal therapy, reporting no serious adverse events (SAE).

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AIM reports positive safety data from intranasal Covid-19 drug trial

8 April 2021 (Last Updated April 8th, 2021 08:00) AIM ImmunoTech has reported that no serious adverse events were observed in Cohort 1 of a Phase I AMP-COV-100 (CHDR2049) clinical study of its drug Ampligen as an intranasal therapy for Covid-19. With this latest development, the company will soon initiate dose escalation in Cohort 2 of the trial. Credit: Gerd Altmann from Pixabay. Share Article AIM ImmunoTech has reported that no serious adverse events were observed in Cohort 1 of a Phase I AMP-COV-100 (CHDR2049) clinical study of its drug Ampligen as an intranasal therapy for Covid-19. With this latest development, the company will soon initiate dose escalation in Cohort 2 of the trial.

Thomas equelsCentre for human drug researchPlacebo controlled studyRepeated intranasal administrationHealthy subjectsHuman drug researchMembrane vesicleமையம் க்கு மனிதன் மருந்து ஆராய்ச்சிமருந்துப்போலி கட்டுப்படுத்தப்படுகிறது படிப்புஆரோக்கியமான பாடங்கள்மனிதன் மருந்து ஆராய்ச்சி

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

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AIM ImmunoTech Inc reports no serious adverse events in dosing of Cohort 1 in a Phase 1 clinical study on the safety of its Ampligen drug as an intranasal therapy

AIM ImmunoTech Inc reports no serious adverse events in dosing of Cohort 1 in a Phase 1 clinical study on the safety of its Ampligen drug as an intranasal therapy
proactiveinvestors.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from proactiveinvestors.com Daily Mail and Mail on Sunday newspapers.

Thomas equelsCentre for human drug researchHuman drug researchமையம் க்கு மனிதன் மருந்து ஆராய்ச்சிமனிதன் மருந்து ஆராய்ச்சி