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OCALA, Fla., Feb. 16, 2021 (GLOBE NEWSWIRE) AIM ImmunoTech Inc. (NYSE American: AIM) today announced that it has received approval from the required Ethics Committee in the Netherlands to commence its Phase 1 clinical study on the safety of AIM s drug Ampligen as an intranasal therapy, 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.
Earlier this year, the company announcedthat it had entered into a sponsorship agreement with the Centre for Human Drug Research (CHDR) for the proposed AMP-COV-100 (CHDR2049) trial. Last week, approval was received from the Dutch local Ethics Committee, clearing the road for execution of the trial.
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AIM ImmunoTech Inc receives required Ethics Committee approval in the Netherlands to commence its Phase 1 clinical study on the safety of its drug Ampligen as an intranasal therapy
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AIM ImmunoTech forms sponsorship agreement of Ampligen as intranasal therapy for the coronavirus
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Entheon Biomedical Corp.: Entheon Biomedical Provides Update on Centre for Human Drug Research License Amendments Entheon or the Company ), a biotechnology company focused on developing psychedelic medicines to treat addiction, provides an update on license amendments issued to its clinical research organization, The Centre for Human Drug Research (CHDR).
Entheon confirms that the CHDR, the Company s Netherlands-based partner clinical research organization, has received an amendment to its opioid license, enabling it to possess and conduct research with DMT. The opioid license amendment enables the CHDR to accommodate Entheon s upcoming clinical study, designed to evaluate the pharmacodynamics, pharmacokinetics and safety of a target-controlled IV infusion of DMT in humans. In addition, CHDR s partner pharmacy, LUMC, has received its import permit to receive DMT, for testing and formulation work, from Entheon s Canadian manufacturing partner, Psygen Labs Inc.