Royalty Report: Drugs, Drug Discovery, Diagnostic – Collection: 380857

$150.00

Curated Royalty Rate Report
Category: Technology Licenses, Created On: 2022-04-28, Record Count: 7

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: 7

Primary Industries

  • Drugs
  • Drug Discovery
  • Diagnostic
  • Pain
  • Nerve
  • Technical Know How
  • Bacterial Infection
  • Disease
  • Central Nervous System
  • Delivery
  • Therapeutic
  • 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: 380857

License Grant
This Agreement expands the field of the license granted to all indications and to make certain other changes.

Licensor grants to the Licensee of France an exclusive license, with the right to sublicense, under the Licensor Patents claiming such Licensor Information, and to use such Licensor Information, in each case to develop, register, manufacture, use, distribute, sell, offer for sale and have sold the Licensor Product in the Rest of the World in such indication within the Field.

License Property
Licensed Product shall mean any product, including a Licensee Product or product containing a Licensor Formulation, containing Milnacipran as an active ingredient, in any formulation and through any mode of administration, that incorporates or uses the Licensed Technology or the manufacture, use or sale of which is within the scope of any claim of the Licensee Patents
—  the immediate release formulation in capsule form containing 25 mg and 50 mg of Milnacipran (the IR Formulation), and
—  the slow release formulation covered by Pierre Fabre Patents containing 120 mg of Milnacipran (the SR Formulation).

Licensors patents include
Methods of treating fibromyalgia syndrome;
Methods of treating Chronic Fatigue Syndrome;
Methods of treating attention deficit hyperactivity disorder;
Methods of treating visceral pain syndromes;
Methods of treating functional somatic disorders;
Methods of assessing the level of a subjective symptom;
Treatment of Pain Associated Depression;
Dosage escalation of Milnacipran;
Treatment of Sleep Disorders;
Increased and divided daily dosage of anti-depressant to treat pain and functional somatic symptons; and,
Treatment of cognitive disfunctions.

Field of Use
The initial agreement field of use for Milnacipran is for the treatment of depression.  In this restated agreement FMS shall mean the prevention and treatment of fibromyalgia syndrome.

By this restated agreement, Field shall mean any and all indications.

IPSCIO Record ID: 372573

License Grant
This Agreement expands the field of the license granted to all indications and to make certain other changes.

Licensor of France grants an exclusive license, with the right to sublicense, under the Licensed Technology to develop, register, use, distribute, sell, offer for sale, have sold and import the Licensed Product in the Licensed Territory in the Field.

Licensor further grants a license to use Licensor Know-How and Licensor Patents, to the extent necessary to formulate or have the API formulated into Bulk Licensed Product and package Bulk Licensed Product into Finished Licensed Product, solely for sale of Licensed Product in the Licensed Territory.

Licensee shall develop the Licensed Product in the Licensed Territory at its own expense, and in accordance with the initial development plan, and, Licensee shall also use commercially reasonable efforts to achieve the following events with respect to a Licensed Product in  fibromyalgia syndrome or FMS in the United States.

License Property
Licensor owns or controls certain patents and valuable know-how related to the compound Milnacipran and the Licensed Product in the form of an IR Formulation and a SR Formulation.

Licensed Product shall mean any product, including a Licensee Product or product containing a Licensee Formulation, containing Milnacipran as an active ingredient, in any formulation and through any mode of administration, that incorporates or uses the Licensed Technology or the manufacture, use or sale of which is within the scope of any claim of the Licensor Patents
—  the immediate release formulation in capsule form containing 25 mg and 50 mg of Milnacipran (the IR Formulation), and
—  the slow release formulation covered by Pierre Fabre Patents containing 120 mg of Milnacipran (the SR Formulation).

Field of Use
The initial agreement field of use for Milnacipran is for the treatment of depression.  In this restated agreement FMS shall mean the prevention and treatment of fibromyalgia syndrome.

Fibromyalgia is a disorder characterized by widespread musculoskeletal pain accompanied by fatigue, sleep, memory and mood issues. Researchers believe that fibromyalgia amplifies painful sensations by affecting the way your brain and spinal cord process painful and nonpainful signals.

By this restated agreement, Field shall mean any and all indications.

IPSCIO Record ID: 203476

License Grant
The parties entered into a relationship whereby Licensor would develop reformulations of milnacipran and analogs of milnacipran, with a patient acceptance profile comparable or superior to the current formulations of milnacipran, pursuant to the terms and conditions of this Agreement.

Licensee hereby grants to Licensor during the R&D Term a non-exclusive, non-sublicensable, non-transferable license to the Licensee for use by Licensor only for the performance of its obligations under this Agreement. Licensor agrees that it shall not use the Licensee for any other purposes.

License Property
Licensor has expertise in developing reformulations of existing products and new products which are analogs of existing products

Licensee Patents shall mean, to the extent necessary or useful for the development of Reformulated Products or New Products or otherwise for purposes of the R&D Plan, (a) all foreign and domestic (i) patents issued or existing as of the Effective Date which Licensee Controls; (ii) patents issuing from patent applications that are pending as of the Effective Date.

Reformulated Product shall mean any Product which is developed by Licensor under this Agreement and contains milnacipran in a formulation that is different than the Existing Product, but that does not meet the criteria for a New Product.

Milnacipran is immediate release formulation in capsule form containing 25 mg and 50 mg of milnacipran and the existing slow release fo1mulation containing 120 mg of milnacipran, as set forth in PCT published international application WO 98/08495.

Field of Use
Milnacipran is used to treat pain caused by a condition called fibromyalgia that affects the muscles, tendons, ligaments, and supporting tissues.  Fibromyalgia is a disorder characterized by widespread musculoskeletal pain accompanied by fatigue, sleep, memory and mood issues. Researchers believe that fibromyalgia amplifies painful sensations by affecting the way your brain processes pain signals.

IPSCIO Record ID: 367296

License Grant
Licensor (a nonprofit, tertiary, hospital and multispecialty academic health science center) hereby grants to Licensee, and Licensee hereby accepts from Licensor, the exclusive license, with the right to grant sublicenses, under and to the Patent Rights and Technical Information during the term of this Agreement to conduct research in the Field of Use and to make, have made, use, develop, import, have imported, export, have exported, offer for sale, or have offered for sale, sell and/or have sold Licensed Products and Licensed Technology Products in the Field of Use in the Territory. The foregoing grant of exclusivity is made expressly subject to the following

(a) All applicable laws and regulations, including, without limitation, the requirements of federal law as pertain to the manufacture of products within the United States;

(b) All applicable rules of the Funding Agencies which have provided funding to Licensor or to any of its employees (including any of the Inventors) for the development of the Patent Rights and Technical Information; and

(c) The following non-exclusive rights to the Patent Rights and Technical Information, which are retained by Licensor within the Field of Use
(i)  the right to submit for publication the scientific findings from research conducted by or through Licensor or its investigators (including the Inventors) related to the Patent Rights and the Technical Information; and
(ii)  the right (A) to use any tangible or intangible information contained in the Patent Rights or the Technical Information or any Improvements (so long as Licensor shall treat such information as Confidential Information and maintain its confidentiality in accordance with Section 10 hereof), for Licensor’s internal non-commercial scientific, research, internal teaching, non-profit clinical research and other educationally-related and non-commercial (except for charges to its own patients) clinical purposes, where clinical use does not involve a third party funding grant to commercialize such information, and (B) to obtain research funding for further study and development thereof from governmental and other nonprofit organizations (including grant applications).

(d) Notwithstanding any other provision hereof to the contrary, all rights to the Patent Rights, Technical Information and Improvements outside of the Field of Use are retained by Licensor. Furthermore, this Agreement confers no license or rights by implication, estoppel, or otherwise under any patent applications or patents of Licensor other than Patent Rights regardless of whether such patents are dominant or subordinate to Patent Rights.

License Property
Patent Rights
6,861,053 – Methods of diagnosing or treating irritable bowel syndrome and other disorders caused by small intestinal bacterial overgrowth

6,805,852 – Methods of diagnosing irritable bowel syndrome and other disorders caused by small intestinal bacterial overgrowth

7,056,686 – Method of diagnosing fibromyalgia caused by small intestinal bacterial overgrowth

Field of Use
Licensed Products relate to new treatment approaches to target non-bacterial intestinal microorganism life forms known as archaea that are associated with intestinal methane production and chronic diseases such as irritable bowel syndrome (IBS), obesity and type 2 diabetes.

Archaea is a group of primitive prokaryotes that based on their distinct characteristics form a separate domain from bacteria and eukaryotes. Bacteria are single-celled primitive organisms that form a domain of organisms diverse in shape, size, structure, and even habitats.

IPSCIO Record ID: 266736

License Grant
Licensor, a non-profit hospital, grants to Licensee to the extent of the Licensed Territory an exclusive license under the patent rights to make, have made, use, sell and have sold, and import licensed products in the Licensed Field, with the right to sub license.

Licensor grants to the extent of the Licensed Territory a nonexclusive license to use the Licensed Technology as necessary to exploit all rights granted with respect to the patent rights in the Licensed Field, with the right to sublicense.

License Property
Licensor owns US Patent application for Methods of Treating Irritable Bowel Syndrome and Other Disorders Caused by Small Intestinal Bacterial Overgrowth, and, US Patent entitled Methods of Diagnosing or Treating Irritable Bowel Syndrome and Other Disorders Caused by Small Intestinal Bacterial Overgrowth.

Rifaximin means rifaximin, any pharmaceutical equivalents, salts and derivatives thereof.

Field of Use
Rifaximin is an antibiotic used to treat traveler's diarrhea, irritable bowel syndrome, and hepatic encephalopathy.

IPSCIO Record ID: 315667

License Grant
The Swiss Licensee obtained a worldwide, sub-licensable license from the Licensor covering four different compounds, which included Mazindol (the “Licensed Compounds”). Under the Second Amendment it was agreed to include sales realized upon the commercialization of products developed on the basis of the Licensed Compounds during the terms of their respective patents.  The Licensee’s majority shareholders are also majority shareholders in the Licensor and as such are considered to be related parties.
License Property
Licensed Compound, Mazindol, is an active molecule in a proprietary controlled release formulation. The controlled-release formulations are being designed to optimize their pharmacokinetic and pharmacodynamic properties with a rapid onset of action and prolonged controlled therapeutic effect, allowing for a daily oral dose that effectively provides consistent and long acting symptom control and designed to uniquely meet the needs of patients.

Licensor is primarily focusing on the repurposing of safe and (cost-)effective compounds to treat Attention Deficit/HyperActivity Disorder (ADHD), sleep disorders and cognitive impairment.

Field of Use
Licensee will utilize Mazindol, an active substance, to cover a range of areas including the therapeutic use of mazindol for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) and combination therapies containing mazindol (add-ons with iron or stimulants) as well as sleep disorders such as narcolepsy or idiopathic hypersomnia.  Attention Deficit Hyperactivity Disorder (ADHD) is a group of behavioral symptoms that include inattentiveness, hyperactivity and impulsiveness.

Licensee is an innovative biotechnology company engaged in the discovery and development of life-improving drug therapies to treat rare and complex central nervous system, or CNS, disorders, including narcolepsy, idiopathic hypersomnia and other rare sleep disorders, and of neurodevelopmental disorders, such as Attention Deficit Hyperactivity Disorder, or ADHD. CNS disorders are a diverse group of conditions that include neurological, psychiatric, and substance use disorders.

IPSCIO Record ID: 25935

License Grant
French Licensor hereby grants to Licensees during the License Term, an exclusive license, with the right to sub-license subject to develop, register, use, distribute, sell, offer for sale, have sold and import the Licensed Product in the Licensed Territory in the Field, which license shall be under the Licensed Technology. Licensor further grants Licensee a license to use Licensed Technology, to the extent necessary to formulate or have the API formulated into Bulk Licensed Product and package Bulk Licensed Product into Finished Licensed Product, solely for sale of Licensed Product in the Licensed Territory.

Pursuant to this agreement, the parties agree to a royalty payment for the right to sublicense the technology. French Licensor hereby grants.

License Property
Licensor owns or controls certain patents and valuable know-how related to the compound Milnacipran and the Licensed Product.

Licensor has developed Milnacipran for the treatment of depression and currently markets the IR Formulation itself or through licensees for the treatment of depression in certain territories outside the United States.

Field of Use
Milnacipran is a serotonin and norepinephrine reuptake inhibitor (SNRI) which was first approved for the treatment of major depressive episodes.
Disclaimer: The information gathered from RoyaltySource® database was sourced from the U.S. Securities and Exchange Commission EDGAR Filings and other public records. While we believe the sources to be reliable, this does not guarantee the accuracy or completeness of the information provided. Further, the information is supplied as general guidance and is not intended to represent or be a substitute for a detailed analysis or professional judgment. This information is for private use only and may not be resold or reproduced without permission.