Royalty Report: Drugs, Antibody, Biotechnology – Collection: 56588

$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
  • Antibody
  • Biotechnology
  • Cancer
  • Agriculture Forestry & Fishing
  • Crop Production
  • Proteins
  • Disease
  • Vaccine
  • Agriculture
  • Forestry and Fishing
  • Technical Know How
  • DNA
  • cell therapy

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: 56588

License Grant
In this related party agreement, the Licensor hereby grants to Licensee a nonexclusive license in the Territory, with the right to sublicense, to use iBioLaunchâ„¢ Technology and iBio Additional Technology to conduct Process Development, Scale-Up, and R&D activities on Pharmaceutical Products in the Territory. Additionally, subject to the terms and conditions of this Agreement, Licensor hereby grants to Licensee a nonexclusive license in the Territory, with the right to sublicense, to use the iBio Additional Technology to conduct Process Development, Scale-Up, and R&D activities on Products in the Territory.
License Property
The patents and technology are for the accelerated discovery and production of improved vaccines, monoclonal antibodies, therapeutic proteins, and other products derived from green plants utilizing its iBioLaunchâ„¢ plant-based platform technology and other proprietary technologies.

7,012,172   VIRUS INDUCED GENE SILENCING IN PLANTS   3/14/2006
          
7,491,509   SYSTEM FOR EXPRESSION OF GENES IN PLANTS   2/17/2009
          
7,683,238   PRODUCTION OF PHARMACEUTICALLY ACTIVE PROTEINS IN SPROUTED SEEDLINGS   3/23/2010
          
7,692,063   PRODUCTION OF FOREIGN NUCLEIC ACIDS AND POLYPEPTIDES IN SPROUT SYSTEMS   4/6/2010
          
8,058,511   SYSTEM FOR EXPRESSION OF GENES IN PLANTS   11/15/2011
          
8,148,608   SYSTEMS AND METHODS FOR CLONAL EXPRESSION IN PLANTS   4/3/2012
          
8,173,408   RECOMBINANT CARRIER MOLECULE FOR EXPRESSION, DELIVERY AND PURIFICATION OF TARGET POLYPEPTIDES   5/8/2012
          
8,591,909   RECOMBINANT CARRIER MOLECULE FOR EXPRESSION, DELIVERY AND PURIFICATION OF TARGET POLYPEPTIDES   11/26/2013
          
8,597,942   SYSTEM FOR EXPRESSION OF GENES IN PLANTS   12/3/2013
          
8,951,791   SYSTEM FOR EXPRESSION OF GENES IN PLANTS   2/10/2015
          
9,012,199   RECOMBINANT CARRIER MOLECULE FOR EXPRESSION, DELIVERY AND PURIFICATION OF TARGET POLYPEPTIDES   4/21/2015

Field of Use
This agreement pertains to the patents and technologies for research, process development and scale-up, and manufacturing of plant-derived products in a manufacturing facility designed for that purpose relating to drugs in the healthcare industry.

IPSCIO Record ID: 26281

License Grant
The Licensee and Licensor (our collaborative research and development partners) completed the Terms of Settlement for the TTA Seventh Amendment.  This agreement has the effect of further amending the terms of the Technology Transfer Agreement originally entered into effective as of January 1, 2004 the significant terms of which are as follows

The Licensee’s liabilities to Licensor were released and terminated;  The Licensee’s obligation under the TTA, prior to the Settlement Agreement, to make payments to Licensor in April 2013, November 2013, and April 2014 (the Guaranteed Annual Payments) was terminated and replaced with an obligation to engage Licensor to perform research and development work. Any and all other claims of each party to any other amounts due at June 30, 2013 were mutually released. The Licensee will continue to make royalty payments to the Licensor.

License Property
iBioModulator is a proprietary technology platform that is designed to improve the potency and duration of effect of both prophylactic and therapeutic vaccines produced with any recombinant expression technology including iBioLaunch. Stated simply, iBioLaunch harnesses the natural protein production capability that plants use to sustain their own growth, and directs it instead to produce proteins that comprise the active pharmaceutical ingredients in vaccines and biopharmaceuticals. The Licensee pipeline includes vaccines, enzyme replacements, monoclonal antibodies, and recombinant versions of marketed products that are currently derived from human blood plasma.
Field of Use
The Licensee is a biotechnology company focused on commercializing the proprietary platform technologies, iBioLaunchâ„¢ and iBioModulatorâ„¢. iBioLaunch is a transformative platform technology for development and production of biologics using transient gene expression in hydroponically grown, unmodified green plants.

IPSCIO Record ID: 6483

License Grant
Licensor grants the following licenses and rights under Licensor Technology
—  a world-wide, co-exclusive, with Licensor, research license under Licensor Technology to use ZFP Products in the Field for research purposes and to make and test Licensed Products for research purposes;
—  the exclusive right to grant research licenses to Third Parties to use ZFP Products in the Field for research purposes and to make and test Licensed Products for research purposes; and,
—  the exclusive right to grant to Sublicensees a license to use ZFP Products in the Field for the sole purpose of generating Licensed Products and, to use, make, offer to sell, sell, and import such Licensed Products.

For Additional Grants to Licensee Effective after Exercise of Option, the following additional licenses and rights under Licensor Technology are
—  a world-wide, exclusive license to make, use, and import ZFP Products for use in the Field, which Licensee shall exercise for the sole purposes of generating Licensee Products; or offering for sale and selling ZFP Products at cost to Sublicensees for use in the Field for the sole purpose of generating Licensed Products;
—  a world-wide, exclusive license to make, use, sell, offer for sale, and import Licensee Products.

For Non-exclusive rights for Animal Health Products and Human Health Products, each of the licenses and rights granted shall be non-exclusive with respect to Animal Health Products and Human Health Products.

Licensor hereby grants the exclusive right to grant to Sublicensees a license (A) to use ZFP Products in the Field for the sole purpose of generating Licensed Products and (B) to use, make, offer to sell, sell, and import such Licensed Products, all pursuant to Technology Licenses.

License Property
Licensor technology includes Directory of zinc finger designs, archive of two-finger modules, and others regarding methods for synthesis and assaying related proteins and nucleic acids.

Through the initial agreement the Licensee has access to our proprietary zinc finger DNA-binding protein (ZFP) technology and the exclusive right to use ZFP technology to modify the genomes or alter the nucleic acid or protein expression of plant cells, plants, or plant cell cultures. The Licensor has retained rights to use plants or plant-derived products to deliver ZFP transcription factors (ZFP TFsâ„¢) or zinc-finger nuclease (ZFNâ„¢) into human or animals for diagnostic, therapeutic, or prophylactic purposes.

ZFP Product means a zinc-finger protein, including a zinc-finger transcription factor or a zinc-finger nuclease, or a nucleic acid encoding and capable of expressing such protein in a cell or tissue.

Stacking Crop Product means a Crop Product that is a Licensee Product, is the direct or indirect result of using one or more ZFP Products to produce a plant or plant cell comprising Traits, where these Traits were each available in separate plants or plant cells that could have been crossed to produce a breeding stack of the two Traits, and is not the result of any other activity in the Field.

Field of Use
The Licensee exercised its option under the Exclusive License Agreement that was Effective October 2005, to obtain a commercial License to sell products incorporating, or derived from, plant cells generated using the Licensor's ZFP technology, including agricultural crops, industrial products and plant-derived biopharmaceuticals. The research program has been extended beyond the initial three-year research term and the Licensee is providing additional research funding.

Field means gene targeting and/or gene regulation using a ZFP Product to modify the genome of a plant cell, plant, or plant cell culture (in each case, whether constituting or derived from a vascular or non-vascular plant), or alter the nucleic acid or protein expression in a plant cell, plant, or plant cell culture. For the purpose of this Agreement, non-vascular plants shall include but not be limited to algae, moss, and fungi. Explicitly excluded from the Field are delivery of any ZFP Product into a human or animal for diagnostic, therapeutic or prophylactic purposes, and products intended to result in such delivery.

IPSCIO Record ID: 202855

License Grant
Licensor grants to Licensee under all Licensors Patents a nonexclusive, worldwide, sublicensable license to the extent necessary to make, have made, use, sell, have sold and import Licensees Licensed Products for the treatment, prophylaxis or diagnosis of any disease or condition in humans and animals; provided, however, that with respect to Licensees Licensed Products containing an Anti-IgE Antibody identified and synthesized before June 1, 1997, and/or Licensors Patents issued before June 1, 1999, the foregoing limitation -to the extent necessary- shall not be applicable.
License Property
Anti-IgE Antibody means an antibody directed against the immunoglobulin IgE as an antigen, fragments or conjugates of such antibodies, and other constructs comprising antibodies which are derived from or contain any of the above-specified components.

Licensees Licensed Product means any pharmaceutical formulation or product or method or system which contains an Anti-IgE Antibody.

Licensors Licensed Product means any pharmaceutical formulation or product or method or system which contains an Anti-IgE Antibody identified and synthesized by Licensor and/or a third party, or other IgE inhibiting antibodies within Licensorss MIGIS(R) program.

Field of Use
The agreement is for antibodies for immunology, infectious diseases and cancer.

IPSCIO Record ID: 256278

License Grant
On the Effective Date the Parties have terminated a certain Collaboration Agreement, and with this agreement, the Parties desire to reallocate the rights and responsibilities of the Parties with respect to further research and development of the GM-CSF Target.

Licensor grants to Licensee of Germany an exclusive, worldwide, license under the Licensor Licensed Technology to Exploit Licensed Products.

Licensor grants a worldwide, non-exclusive, perpetual, irrevocable and non-terminable license under the Collaboration Patents, as defined in the Collaboration Agreement, with the right to grant and authorize the grant of sublicenses, to Exploit Licensed Products.

License Property
BiTE Product means any composition or formulation consisting of or comprising a bi-specific Single Chain Antibody expressed as a single polypeptide chain, binding to T-cells.

GM-CSF Target means the whole or part of the human granulocyte macrophage-colony stimulating factor identified by the SWISS-PROT entry name CSF2 HUMAN and accession number P0414 l.

Single-Chain Antibodies
Antibodies are proteins produced by the body's immune system in response to the presence of antigens, such as bacteria, viruses or other disease causing agents. Antibodies of identical molecular structure that bind to a specific target are called monoclonal antibodies. Single-chain antibodies are genetically engineered antibodies that incorporate only the antigen binding domains of an antibody. Thus, SCAs have the binding specificity and affinity of monoclonal antibodies; however, in their native form they are only one-fifth to one-sixth the size of a monoclonal. The small size of SCAs typically gives them shorter half-lives than monoclonal antibodies, making them better suited for use in acute indications or in other indications where the large size of a monoclonal antibody would inhibit the compound from reaching the area of potential therapeutic activity. In addition, SCAs are a well-established discovery format-of-choice in generating antibodies from phage or yeast display libraries.

Field of Use
The field for Patent 5,223,409 is solely in the field of manufacture, use or sale of Single Chain Antibodies.

The field of use for this agreement otherwise is limited to not include the right to exploit the Products for Radioimmunoguided Surgery(TM), Reagents and kits in the research market for production and cloning of genes encoding Single Chain Antibodies and their fusions in a filamentous bacteriophage-derived vector system, and for expression and screening of Single Chain Antibodies fused with the minor coat protein or attachment or adsorption protein of filamentous bacteriophage, and, Single Chain Antibodies fused with, or for the assay or purification of, Tumor Necrosis l Factor alpha (TNF-a.) or Lymphotoxin.

Products for Radioimmunoguided SurgeryTM (RIGS'), in which a radiolabelled Single Chain Antibody is administered to a cancer patient; time elapses for preferential concentration of the radiolabelled Single Chain Antibody in neoplastic tissue and decrease of background radioactivity in the patient; and such preferentially concentrated radiolabelled Single Chain Antibody is detected within a surgical operative field by a detector probe placed in juxtaposition with tissue suspected of containing said radiolabelled Single Chain Antibody.

IPSCIO Record ID: 121012

License Grant
Pursuant to this Settlement and Cross-license agreement, Licensor grants to Licensee of Bermuda under all Licensor Patents, on a country-by-country basis in the Licensees Territory, an exclusive, sublicenseable license to make, have made, use, sell, have sold and import Licensees Licensed Products for the treatment, prophylaxis or diagnosis of any disease or condition in humans;  with respect to Licensees Licensed Products containing an Anti-IgE Antibody identified and synthesized before June 1, 1997, and/or Licensors Patents issued before June 1, 1999.
License Property
Anti-IgE Antibody means an antibody directed against the immunoglobulin IgE as an antigen, fragments or conjugates of such antibodies, and other constructs comprising antibodies which are derived from or contain any of the above-specified components.

Licensees Licensed Product means any pharmaceutical formulation or product or method or system which contains an Anti-IgE Antibody.

Licensors Licensed Product means any pharmaceutical formulation or product or method or system which contains an Anti-IgE Antibody identified and synthesized by Licensor and/or a third party, or other IgE inhibiting antibodies within Licensorss MIGIS(R) program.

Field of Use
The agreement is for the drug industry relating to antibodies for immunology, infectious diseases and cancer.

IPSCIO Record ID: 204997

License Grant
Licensor grants
– a worldwide, exclusive, to the extent such exclusivity is possible in the light of  existing agreements, license to make, have made, use and sell Specialty Canola Products and Specialty High Stearate Canola Products using Licensor Patent Rights, with rights to sublicense,
– a worldwide, non-exclusive license to make, have made, use and sell Commodity Canola Products and Commodity High Stearate Canola Products using Licensor Patent Rights, without the right to sublicense
– a worldwide, non-exclusive license, with no right to sublicense, to make, have made and use, for research purposes only, oilseed products other than Commodity Canola Products, Commodity High Stearate Canola Products, Specialty Canola Products and Specialty High Stearate Canola Products using Licensor Patent Rights, and  
– for Specialty Canola Products and Specialty High Stearate Canola Products, the limited right to sublicense only transgenic plant germplasm produced by Licensee, with the right to develop, use and sell new varieties and/or hybrids produced therefrom by traditional plant breeding, containing genes developed or in-licensed by Licensee to any Third Party or Licensee Affiliate.
License Property
Licensor has proprietary rights to certain technology applicable to the engineering of plants and in plant expression, as well as technology for introducing agronomic traits, which is useful in the improvement of oilseeds and in modifying oil composition.

Agronomic Genes shall mean genes encoding for disease resistance, herbicide tolerance, cold tolerance, shatter resistance, yield improvement,  earliness,  insect  tolerance,  drought  resistance  and heat resistance and other genes that reduce the net unit cost of production of agricultural crop plants.

The patents relate to Increased starch content in Plants and Expression of Sucrose Phosphorylase in Plants.

Field of Use
This agreement is for the agriculture production industry.
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