Year
DEALS // DEV.
Country
Therapeutic Area
Study Phase
Deal Type
Product Type
Dosage Form
Lead Product
Target
AZURITY Wins FDA Approval for DANZITEN™ Tablets with No Mealtime Restrictions
Details : Danziten (nilotinib), an oral BCR-ABL kinase inhibitor, it is indicated for treating adult patients with newly diagnosed Philadelphia chromosome positive chronic myeloid leukemia.
Brand Name : Danziten
Molecule Type : Small molecule
Upfront Cash : Not Applicable
November 14, 2024
Lead Product(s) : Nimodipine
Therapeutic Area : Neurology
Study Phase : Approved
Sponsor : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
Azurity Pharmaceuticals’ NYMALIZE® Oral Solution Approved by FDA
Details : Nymalize is a clinical stage, novel formulation of nimodipine, a calcium channel blocker, approved for treating aneurysmal subarachnoid hemorrhage patients.
Brand Name : Nymalize
Molecule Type : Small molecule
Upfront Cash : Not Applicable
September 03, 2024
Lead Product(s) : Nimodipine
Therapeutic Area : Neurology
Highest Development Status : Approved
Sponsor : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
Lead Product(s) : Mycophenolate Mofetil
Therapeutic Area : Immunology
Study Phase : Approved
Sponsor : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
Azurity Announces FDA Approval Of Myhibbin™ Oral Suspension
Details : Myhibbin (mycophenolate mofetil) is an immunosuppressive agent acting as an inosine monophosphate dehydrogenase (IMPDH) inhibitor, indicated for preventing organ rejection in transplant patients.
Brand Name : Myhibbin
Molecule Type : Small molecule
Upfront Cash : Not Applicable
May 06, 2024
Lead Product(s) : Mycophenolate Mofetil
Therapeutic Area : Immunology
Highest Development Status : Approved
Sponsor : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
Lead Product(s) : Dexmedetomidine Hydrochloride
Therapeutic Area : Neurology
Study Phase : Approved
Recipient : Slayback Pharma
Deal Size : Undisclosed
Deal Type : Acquisition
Azurity Pharmaceuticals Acquires Slayback Pharma
Details : Through the acquisition, Azurity gains access to Slayback's pipeline including, Precedex (dexmedetomidine hydrochloride), an alpha2-adrenergic agonist with sedative properties used for short-term intravenous sedation.
Brand Name : Precedex-Generic
Molecule Type : Small molecule
Upfront Cash : Undisclosed
September 27, 2023
Lead Product(s) : Dexmedetomidine Hydrochloride
Therapeutic Area : Neurology
Highest Development Status : Approved
Recipient : Slayback Pharma
Deal Size : Undisclosed
Deal Type : Acquisition
Lead Product(s) : Omeprazole,Sodium Bicarbonate
Therapeutic Area : Gastroenterology
Study Phase : Approved
Recipient : Brand Institute
Deal Size : Not Applicable
Deal Type : Not Applicable
Details : KONVOMEP™ (omeprazole and sodium bicarbonate for oral suspension) is a medication indicated for short-term treatment (4 to 8 weeks) of active benign gastric ulcer and reduction of risk of upper gastrointestinal bleeding in critically ill adult patients...
Brand Name : Konvomep
Molecule Type : Small molecule
Upfront Cash : Not Applicable
September 07, 2022
Lead Product(s) : Omeprazole,Sodium Bicarbonate
Therapeutic Area : Gastroenterology
Highest Development Status : Approved
Recipient : Brand Institute
Deal Size : Not Applicable
Deal Type : Not Applicable
Lead Product(s) : Omeprazole,Sodium Bicarbonate
Therapeutic Area : Gastroenterology
Study Phase : Approved
Sponsor : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
Details : Konvomep™ (omeprazole and sodium bicarbonate for oral suspension) is approved for the treatment of active benign gastric ulcer and reduction of risk of upper gastrointestinal bleeding in critically ill patients.
Brand Name : Konvomep
Molecule Type : Small molecule
Upfront Cash : Not Applicable
September 02, 2022
Lead Product(s) : Omeprazole,Sodium Bicarbonate
Therapeutic Area : Gastroenterology
Highest Development Status : Approved
Sponsor : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
Lead Product(s) : Brimonidine Tartrate
Therapeutic Area : Ophthalmology
Study Phase : Phase III
Sponsor : Dr. Reddy\'s Laboratories
Deal Size : Undisclosed
Deal Type : Licensing Agreement
Details : Slayback’s Brimonidine Tartrate Ophthalmic Solution 0.025%, the private label equivalent of Lumify® in U.S. Lumify® is an over-the-counter (OTC) eyedrop that can be used to relieve redness of the eye due to minor eye irritations.
Brand Name : Brimonidine Tartrate-Generic
Molecule Type : Small molecule
Upfront Cash : Undisclosed
July 29, 2022
Lead Product(s) : Brimonidine Tartrate
Therapeutic Area : Ophthalmology
Highest Development Status : Phase III
Sponsor : Dr. Reddy\'s Laboratories
Deal Size : Undisclosed
Deal Type : Licensing Agreement
Lead Product(s) : Brimonidine Tartrate
Therapeutic Area : Ophthalmology
Study Phase : Phase III
Sponsor : Dr. Reddy\'s Laboratories
Deal Size : Undisclosed
Deal Type : Licensing Agreement
Details : Lumify® is an over-the-counter (OTC) eyedrop having Brimonidine Tartrate that can be used to relieve redness of the eye due to minor eye irritations. The agreement also provides Dr. Reddy’s exclusive rights to the product outside the U.S.
Brand Name : Brimonidine Tartrate-Generic
Molecule Type : Small molecule
Upfront Cash : Undisclosed
July 29, 2022
Lead Product(s) : Brimonidine Tartrate
Therapeutic Area : Ophthalmology
Highest Development Status : Phase III
Sponsor : Dr. Reddy\'s Laboratories
Deal Size : Undisclosed
Deal Type : Licensing Agreement
Lead Product(s) : Zonisamide
Therapeutic Area : Neurology
Study Phase : Approved
Sponsor : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
Azurity Pharmaceuticals, Inc. Announces FDA Approval of Zonisade™ (Zonisamide Oral Suspension)
Details : ZONISADE is first and only zonisamide formulation for oral liquid administration to be approved by FDA, as an adjunctive therapy for the treatment of partial seizures in adults and pediatric patients aged 16 years and older with epilepsy.
Brand Name : Zonisade
Molecule Type : Small molecule
Upfront Cash : Not Applicable
July 18, 2022
Lead Product(s) : Zonisamide
Therapeutic Area : Neurology
Highest Development Status : Approved
Sponsor : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
Lead Product(s) : Zonisamide
Therapeutic Area : Neurology
Study Phase : Approved
Recipient : Eton Pharmaceuticals
Deal Size : Not Applicable
Deal Type : Not Applicable
Eton Pharmaceuticals Announces FDA Approval of ZONISADE (Zonisamide Oral Suspension)
Details : Zonisade is the first and only zonisamide formulation for oral liquid administration to be approved by the US Food and Drug Administration as an adjunctive therapy for the treatment of partial seizures in adults and paediatric patients aged 16 years and ...
Brand Name : Zonisade
Molecule Type : Small molecule
Upfront Cash : Not Applicable
July 18, 2022
Lead Product(s) : Zonisamide
Therapeutic Area : Neurology
Highest Development Status : Approved
Recipient : Eton Pharmaceuticals
Deal Size : Not Applicable
Deal Type : Not Applicable
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