Royalty Report: Drugs, Pain, Pharmaceuticals – Collection: 266813

$150.00

Curated Royalty Rate Report
Category: Technology Licenses, Created On: 2022-04-28, Record Count: 6

Description

This collection of transactions and supporting information was developed using our AI algorithm to curate similar royalty reports into a cohesive collection to support your licensing, transfer pricing or other transaction scenarios where documented royalty rates and/or deal terms are important.
Category: Technology Licenses
Created On: 2022-04-28
Record Count: 6

Primary Industries

  • Drugs
  • Pain
  • Pharmaceuticals

IPSCIO Report Record List

Below you will find the records curated into this collection.  This summary includes the complete licensed property description so that you can review and determine if this collection covers the topics, technology or transaction type that is relevant for your needs.  The full report will include all relevant deal data such as the royalty base, agreement date, term description, royalty rates and other deal terms.  For reference, here is a sample of a full IPSCIO curated royalty rate report: Sample Report

IPSCIO Record ID: 266813

License Grant
The Licensor of France grants an exclusive license, with right to sublicense, under the Licensed Rights, lo import, use, sell and offer for sale, make and have made, Products in the Territory.

Licensor also grants the right to make and have made the Products outside the Territory for use within the Territory.

License Property
Injectible APAP Product means any parenterally administered dosage form of paracetamol or propacetamol, or any Derivative thereof, whether alone or in combination with one or more other drugs.

The term Product shall mean any parenterally administered dosage form containing paracetamol.

Paracetamol, also known as acetaminophen and APAP, is a medication used to treat pain and fever. It is typically used for mild to moderate pain relief. There is mixed evidence for its use to relieve fever in children. It is often sold in combination with other medications, such as in many cold medications.

Field of Use
Competing Product means any one or more non-opiate analgesic parenterally-administered liquid solution products, in a stable and readily injectible form for the treatment of post-operative pain.

IPSCIO Record ID: 266812

License Grant
Licensor grants
—  an exclusive, even as to Licensor, royalty-bearing sublicense under the Licensor Rights with the right to sublicense, to import, use, sell and offer for sale Products in the Territory;
—  an exclusive, even as to Licensor, sublicense under the Licensor Rights, with the right to sublicense, to make and have made the Products in the Territory solely for import, use, sale and offer for sale within the territory or import and use in clinical trials in the Clinical Study Countries as permitted; and
—  an exclusive, even as to Licensor, sublicense under the Licensor Rights, with the right to sublicense, to make and have made the Products anywhere in the world solely for import, use, sale and offer for sale within the Territory, subject to the limitations set forth in an Agreement relating to parenteral paracetamol, or import or use in Licensees clinical trials in the Clinical Study Countries as permitted;
—  a non-exclusive license under the Licensors Patents, with the right to sublicense, to import, use, sell and offer for sale Products in the Territory;
—  a non-exclusive license under the Licensor Patents, with the right to sublicense, to make and have made the Products in the Terriitory solely for import, use, sale and offer for sale within the Territory;
—  a non-exclusive license under the Licensor Know-How, with the right to sublicense, to make and have made the Products anywhere in the world solely for use and sale within the Territory and import and use in clinical trials in the Clinical Study Countries as permitted; and,
—  a non-exclusive right to use, copy, translate, display and distribute, improve and make derivative works of the Licensor Technology Documentation for the purpose of making and having made the Products consistent with the license set forth above with respect to the Licensor Know-How.
License Property
Licensor has licensed a civil law partnership organized under the laws of France, rights under certain patents and patent applications relating to parenteral paracetamol.  Parenteral paracetamol is also referred to in the United States as acetaminophen.

Product means any parenterally administered dosage form containing paracetamol, or any Derivative thereof, alone or in combination with one or more other drugs, and for which the manufacture, use or sale in a country in the Territory would otherwise infringe any of the Licensed Patents or Licensors Patents but for the license rights granted by Licensor herein, and/or incorporates or uses to any material extent any Licensed Know-How and/or any parenterally administered dosage form containing paracetamol, or any Derivative thereof, alone or in combination with one or more other drugs that is manufactured by a process that incorporates or uses to any material extent any Licensor Know-How.

Field of Use
Licensee is a biopharmaceutical company focused on in-licensing, developing and commercializing proprietary product candidates principally for use in the hospital setting.

Paracetamol (acetaminophen) is a pain reliever and a fever reducer. The exact mechanism of action of is not known. Paracetamol is used to treat many conditions such as headache, muscle aches, arthritis, backache, toothaches, colds, and fevers.

IPSCIO Record ID: 280936

License Grant
Licensor hereby grants to Licensee on behalf of itself and its Affiliated Companies (A) an exclusive (even as to Licensor), royalty-bearing sublicense under the Licensor Rights with the right to sublicense as provided in this agreement, to import, use, sell and offer for sale Products in the Territory; (B) an exclusive (even as to Licensor) sublicense under the Licensor Rights, with the right to sublicense as provided in this agreement, to make and have made the Products in the Territory solely for (1) import, use, sale and offer for sale within the Territory or (2) import and use in clinical trials in the Clinical Study Countries as permitted, (C) an exclusive (even as to Licensor) sublicense under the Licensor Rights, with the right to sublicense, to make and have made the Products anywhere in the world solely for (1) import, use, sale and offer for sale within the Territory, subject to the limitations set forth in the Pharmatop License Agreement (other than the consent of UPSA S.A., which has been obtained as of the Effective Date) and subject to this agreement, or (2) import or use in Licensee’s clinical trials in the Clinical Study Countries as permitted.

A non-exclusive license under the Licensor Patents, with the right to sublicense as provided in this agreement, to import, use, sell and offer for sale Products in the Territory; provided, however, that the license granted in this paragraph shall not grant any right to the composition of matter of any Other Chemical Entity, or the right to import, use, sell or offer for sale any Other Chemical Entity or to any use not claimed by the Licensor Patents.

A non-exclusive license under the Licensor Know-How, with the right to sublicense as provided in this agreement, to make and have made the Products anywhere in the world solely for (1) use and sale within the Territory and (2) import and use in clinical trials in the Clinical Study Countries as permitted.

A non-exclusive right to use, copy, translate, display and distribute (subject to any confidentiality obligations), improve and make derivative works of the Licensor Technology Documentation for the purpose of making and having made the Products consistent with the license set forth above with respect to the Licensor Know-How.

License Property
Product means (i) any parenterally administered dosage form containing paracetamol (or any Derivative thereof) alone or in combination with one or more other drugs and for which the manufacture, use or sale in a country in the Territory (x) would otherwise infringe any of the Pharmatop Patents or Licensor Patents but for the license rights granted by Licensor hereof, and/or (y) incorporates or uses to any material extent any Pharmatop Know-How and/or (ii) any parenterally administered dosage form containing paracetamol (or any Derivative thereof) alone or in combination with one or more other drugs that is manufactured by a process that incorporates or uses to any material extent any Licensor Know-How. When used with respect to any jurisdiction outside the Territory,

Product shall refer to any parenterally administered dosage form containing paracetamol (or any Derivative thereof) alone or in combination with one or more other drugs.

Pharmatop Patents means the Licensed Patents (as such term is defined in the Pharmatop License Agreement) filed or issued in the Territory and licensed to Licensor under the Pharmatop License Agreement.

U.S. Patent #6,593,331 – Method for treatment of pain
U.S. Patent #6,511,982 – Treatment of pain

Licensor Rights means (i) Licensor’s rights under the Pharmatop Patents and Pharmatop Know-How with respect to the Products in the Territory licensed to Licensor under the Pharmatop License Agreement during the term of this Agreement, subject to the limitations, terms and conditions set forth in the Pharmatop License Agreement and (ii) the right granted to Licensor of the Pharmatop License Agreement to make and have made the Products outside the Territory for use within the Territory.

Field of Use
This agreement pertains to the drug industry relating to the treatment of pain.

IPSCIO Record ID: 4717

License Grant
Licensor hereby grants to Licensee an exclusive license, with the right to grant sublicenses.
License Property
The license is for the development and commercialization of non-injectable Dex (Dexmedetomidine) for use in the treatment of pain (including post-operative pain) in humans in any dosage form for transdermal, transmucosal (including sublingual and intranasal), topical, enteral or pulmonary (inhalational) delivery, the Licensed Dosage Forms, but specifically excluding delivery vehicles for administration by injection or infusion.

Dex is in a class of drugs called alpha-2 adrenergic agonists, which produce their effects by selectively activating the alpha-2 adrenergic receptors in the body and produce a broad range of effects depending on the specific drug and the alpha-receptors it activates, including anti-hypertensive, analgesic and sedative effects. In particular, Dex has demonstrated sedative, analgesic and anxiolytic properties in multiple preclinical and clinical studies, including the new drug application, or NDA, studies for Precedex®.

5217718 & 5124157 TRANSDERMAL ADMINISTRATION OF DEXMEDETOMIDINE – Method and device for administering dexmedetomidine transdermally

Field of Use
Under the Dexmedetomidine License Agreement, they were granted an exclusive license under Licensor Know-How and certain Patents to commercialize products in the territory.

“Field” means the treatment of pain in humans, including mild, moderate, or severe acute and chronic pain, alone or as an adjunct.

IPSCIO Record ID: 26233

License Grant
The royalty bearing transaction is part of an asset purchase agreement between an English and Irish company.  The royalty applies to Phrenilin-related products.
License Property
Phrenilin is butalbital and acetaminophen combination is a pain reliever and relaxant.
Field of Use
Phrenilin is a butalbital/acetaminophen mix that is indicated for relief of tensin headaches without caffeine.

IPSCIO Record ID: 1208

License Grant
Licensor grants an exclusive license under the Technology to Develop, manufacture, have manufactured, import, use and Commercialize Products in the Field in the Territory, including the right to conduct clinical Development of the Products outside the Territory in support of Development and Commercialization of such Products in the Territory, including the right to grant sublicenses.

Licensor grants an exclusive license under the Technology, including foreign counterparts and equivalents of patent rights to the extent any exist, to manufacture and have manufactured Products outside the Territory in order to import, use and Commercialize Products in the Field in the Territory, including the right to grant sublicenses.

Licensor grants an exclusive license to use the Trademarks to Commercialize, including to advertise, promote and distribute, the Products in the Field in the Territory.

Licensor grants an exclusive license to exploit the Domain Names in connection with the Products.

This agreement includes a non-exclusive grant back from Licensee to Licensor.

License Property
Licensor has developed Aversion® Technology and related products intended to deter pharmaceutical product abuse.

Aversion® Composition means a composition having a gel forming polyethylene oxide, sodium lauryl sulfate, and crospovidone.

Product A means an immediate release pharmaceutical product for human use, intended for oral administration in two tablet strengths oxycodone HCl 5.0mg and 7.5mg with each tablet containing the Aversion® Composition with niacin at 30mg.

Product B means an immediate release pharmaceutical product for human use, intended for oral administration in two tablet strengths oxycodone HCl 5.0mg and 10.0mg with each tablet containing the Aversion® Composition with niacin at 30mg and acetaminophen 325mg.

Product C means an immediate release Future Product in three tablet strengths hydrocodone bitartrate 5.0mg, 7.5mg, and 10.0mg with each tablet also containing the Aversion® Composition with niacin at 30mg and acetaminophen 325mg.

Product D means an immediate release Future Product [in three tablet strengths hydromorphone HCl 2.0mg, 4.0mg, and 8.0mg with each tablet also containing the Aversion® Composition with niacin at 30mg.

Trademarks means Aversion®, Acurox™, and Acuracet™.

The patents are for Methods and Compositions for Deterring Abuse of Opioid.

Acurox®, Acuracet® (oxycodone HCI/niacin/APAP) Tablets, Vycavert® (hydrocodone bitartrate/niacin/APAP) Tablets and a fourth undisclosed opioid analgesic product candidate utilizing our proprietary Aversion® Technology.

The Licensee has an option to License in the  territory all future opioid analgesic products developed utilizing Aversion® Technology. The Agreement provides that Licensor or Licensee may develop additional opioid analgesic product candidates utilizing our Aversion® Technology and, if Licensee exercises its option to License such additional product candidates, they will be subject to the milestone and royalty payments and other terms of the Agreement.

The drug is part of a class of opioid analgesic products for treatment for moderate to severe acute pain.

The Licensor is responsible, using commercially reasonable efforts, for all Acurox® Tablet development activities through FDA approval of a 505(b)(2) NDA, for which our expenses are reimbursed to us by the Licensee. After NDA approval the Licensee will be responsible for manufacturing and commercializing Acurox® Tablets in the U.S.

Field of Use
The Field means all present and future indications, as a human therapeutic, for use of the Products for the treatment of pain.
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