Serenity Pharmaceuticals
New York
New York
United States
11 articles about Serenity Pharmaceuticals
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Acerus Announces Amendment and Restatement of the Promissory Note Related to the Up-Front Fee Payable to Former Serenity Securityholders
6/7/2022
Acerus Pharmaceuticals Corporation (the “ Company ” or “ Acerus ”) (TSX:ASP; OTCQB:ASPCD) today announced that it has entered into an amended and restated promissory note (the “ A&R Note ”) covering the up-front fee owed to former Serenity Pharmaceuticals LLC (“ Serenity ”) securityholders.
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Acerus Announces Closing of Acquisition of Serenity Pharmaceuticals LLC and Acquisition of Global Rights to Noctiva™Conference Call to be Held on March 9, 2022 at 8:30am ET to Discuss Transaction
3/7/2022
Acerus Pharmaceuticals Corporation (the “Company” or “Acerus”) (TSX:ASP; OTCQB:ASPCF) today announced the closing of its previously-announced acquisition of Serenity Pharmaceuticals LLC (“Serenity”), including the global rights to its Noctiva™ brand.
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Avadel Pharma Enters Into Exclusive Negotiations With Serenity For Noctiva
8/18/2017
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FDA Approves Serenity’s Noctiva (Desmopressin Acetate) – The First Drug Approved For The Treatment Of Nocturia
3/7/2017
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Serenity Release: FDA Approves First Treatment For Frequent Urination At Night Due To Overproduction Of Urine
3/3/2017
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FDA Panel Expresses Concerns Over Allergan-Serenity Drug for Nighttime Urination
10/18/2016
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CPEX Pharmaceuticals' Partner Serenity Pharmaceuticals Announces Development and Commercialization Agreement with Allergan Inc. for Nocturia Product Candidate
4/1/2010
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Allergan Inc. Licenses Drug for Night-Time Urination; To Pay Serenity Pharmaceuticals $43 Million Upfront; $122 Million in Future Payments
4/1/2010
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CPEX Pharmaceuticals Announces Completion of Phase 2 Trial for Urology Drug by Serenity Pharmaceuticals
2/26/2009
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CPEX Pharmaceuticals Announces Initiation of Phase II Trial for Urology Indication by Serenity Pharmaceuticals
11/17/2008
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CPEX Pharmaceuticals and Serenity Pharmaceuticals Announce Collaboration on Drug Candidate for Urology Indication
8/4/2008