APR Sept/Oct 2023 - 118

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SECTION TITLE
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Pharmaceutical
P.I.N.
Points
Patent Innovation News
Article Title
The purpose of this column is to highlight
and summarize recent key patents in the
pharmaceutical arena issued by the US
Patent Office in June-July, 2023.
Neelam Sharma, MS,
Lakshmi Lavanya Kundurthy, BE and
Hemant N. Joshi, Ph.D., MBA*
Tara Innovations, LLC
www.tara-marketing.com,
*hemantjoshi@tarainnovations.com
Introduction
Paragrapgh Text
Echovirus for Treatment of Tumors;
C. Tong, W. Wang, J. Wan, L. Xu, X. Ye, J.
Zhang and N. Xia; Xiamen University and
Yang Sheng Tang Company Ltd., China;
U.S. Patent # 11,707,496; July 25, 2023.
Current methods like surgery, chemotherapy and radiotherapy
can help cancer patients but may also cause great harm to the
health of patients. The emergence of oncolytic viruses provided a
new therapy to possibly cure malignant tumors. An oncolytic virus
can be described as a genetically engineered or naturally existing
virus that can selectively replicate in cancer cells and then kill
them without damaging the healthy cells. Enteroviruses are one of
kind of oncolytic viruses. The inventors of the present application
found that Echovirus 25 has significant tumor cell killing ability for
specific tumors. The present patent discloses use of an Echovirus
25 (ECHO25) or a modified form thereof, or a nucleic acid molecule
comprising a genomic sequence or cDNA sequence of the ECHO25.
Tri-Specific Binding Molecules
that Specifically Bind to
Multiple Cancer Antigens;
E. Bonvini, P.A. Moore, J. C. Li, L.S.
Johnson and K. Shah; Macrogenics
Inc., USA; U.S. Patent # 11,697,684;
July 11, 2023.
The present invention relates to Tri-Specific Binding
Molecules, which are multi-chain polypeptide molecules
that possess three Binding Domains. These are capable
of mediating coordinated binding to three epitopes - (1)
an epitope of a first Cancer Antigen, (2) an epitope of a
second Cancer Antigen, and (3) an epitope of a molecule
that is expressed on the surface of an immune system
effector cell. This immune-specific binding is capable of
localizing an immune system effector cell to a cell that
expresses a Cancer Antigen, so as to thereby facilitate
the killing of such cancer cell. Generally, the ingredients
of compositions of the invention are supplied either
separately or mixed together in unit dosage form.
Author Name
Author Title
Author Company
Factory-on-a-Chip for Production
of Biologically Derived Medicines/
Biopharmaceuticals/Biologics/
Biotherapeutics;
G. Rao, Y. Kostov, A. Andar, M.Al-Adhami,
S. Deldari, and D. D. Frey; University of Maryland,
USA: U.S. Patent # 11,708,553; July 25, 2023.
Production of biotherapeutics involves a large-scale process chain, which
includes large volume separation, purification, formulation, packaging
and distribution. To counter the complexities and expense, maintain living
organisms, and reduce production time, recent efforts have seen the use
of cellular extracts as a source for biomanufacturing. The present invention
provides for a fully integrated microfluidic system capable of producing
single-dose amounts of biotherapeutics at the point-of-care wherein
protein production, purification and product harvest are all integrated as
a single microfluidic device, which is portable and capable of continuousflow
production of biotherapeutics at the microscale using a cell-free
reaction system. It has a portable " factory-on-a-chip " comprising three
primary components. (i) a microfluidic bioreactor unit for synthesizing
a crude protein, (ii) a microfluidic mixer/de-bubbler unit connected
to the bioreactor unit to dilute the crude protein and remove any air
bubbles during mixing; (iii) a microfluidic purification unit has at least one
purification column to provide the purified protein. This integrated device
comprising a reactor, mixer and purification chip is connected together as
one platform chip.
118 |
| November/December 2021
September/October 2023
http://www.tara-marketing.com

APR Sept/Oct 2023

Table of Contents for the Digital Edition of APR Sept/Oct 2023

INSIDER INSIGHT - From Guidelines to Standards: Why Comprehensive AI Regulation is Essential to Spurring Innovation
BIOPHARMACEUTICAL - Aseptic Process Simulation: Cell and Gene Therapy Manufacture
FORMULATION & DEVELOPMENT - Challenges of Analytical Validation for ATMPs
QC Corner - The Intricacies of Testing for Mycoplasmas in Cell Culture Systems
MICROBIOLOGY - Standardized, Scalable And Efficient: Producing Recombinant Factor C to Quality Standards
FORMULATION AND DEVELOPMENT - R Code to Estimate Probability of Passing USP Dissolution Test
FORMULATION AND DEVELOPMENT - Cloud Computing for Drug Discovery: The Time is Now
CGT CIRCUIT - Navigating the Complex Testing Strategies for Viral Vector-based Gene Therapies
MANUFACTURING - Simplifying Finished Product Manufacturer Site Transfer Variations
FORMULATION AND DEVELOPMENT - Advancing Regulatory Compliance with Natural Language Processing
DRUG DELIVERY - Finding a Greater Vantage Point for Creating Green Therapies
WHITEPAPER - Microbial Testing for the Pharmaceutical Industry
Facility Tour - Eurofins BioPharma Product Testing
ROUNDTABLE - Drug Delivery
MANUFACTURING - Accelerating Biologics R&D with Unified Software and Data Flows
An Interview with Jason Downing, Senior Product Manager, TriLink BioTechnologies®
FORMULATION AND DEVELOPMENT - The Role of Data in the Pharmaceutical Lifecycle
BIOPHARMACEUTICAL - Uniting Quality Expectations on Reinvigorated Biopharma Campuses
WHITEPAPER - VITAMIN C – Tableting with LUBRITAB® RBW Lubricant
WHITEPAPER - Leveraging Analytical Technology Process for CMC
BIOPHARMACEUTICAL - Maximizing the Commercialization Potential of Cell and Gene Therapies
MICROBIOLOGY - Comments on Aseptic Process Simulation (APS) in the New EU GMP Annex 1
VENDOR VIEWPOINT - Continuous & Intervention-Free Microbial Monitoring
APR Sept/Oct 2023 - Cover1
APR Sept/Oct 2023 - Cover2
APR Sept/Oct 2023 - 1
APR Sept/Oct 2023 - 2
APR Sept/Oct 2023 - 3
APR Sept/Oct 2023 - 4
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APR Sept/Oct 2023 - 26
APR Sept/Oct 2023 - 27
APR Sept/Oct 2023 - 28
APR Sept/Oct 2023 - 29
APR Sept/Oct 2023 - 30
APR Sept/Oct 2023 - INSIDER INSIGHT - From Guidelines to Standards: Why Comprehensive AI Regulation is Essential to Spurring Innovation
APR Sept/Oct 2023 - 32
APR Sept/Oct 2023 - 33
APR Sept/Oct 2023 - BIOPHARMACEUTICAL - Aseptic Process Simulation: Cell and Gene Therapy Manufacture
APR Sept/Oct 2023 - 35
APR Sept/Oct 2023 - 36
APR Sept/Oct 2023 - 37
APR Sept/Oct 2023 - 38
APR Sept/Oct 2023 - 39
APR Sept/Oct 2023 - 40
APR Sept/Oct 2023 - 41
APR Sept/Oct 2023 - 42
APR Sept/Oct 2023 - 43
APR Sept/Oct 2023 - FORMULATION & DEVELOPMENT - Challenges of Analytical Validation for ATMPs
APR Sept/Oct 2023 - 45
APR Sept/Oct 2023 - 46
APR Sept/Oct 2023 - 47
APR Sept/Oct 2023 - 48
APR Sept/Oct 2023 - 49
APR Sept/Oct 2023 - QC Corner - The Intricacies of Testing for Mycoplasmas in Cell Culture Systems
APR Sept/Oct 2023 - 51
APR Sept/Oct 2023 - MICROBIOLOGY - Standardized, Scalable And Efficient: Producing Recombinant Factor C to Quality Standards
APR Sept/Oct 2023 - 53
APR Sept/Oct 2023 - 54
APR Sept/Oct 2023 - 55
APR Sept/Oct 2023 - FORMULATION AND DEVELOPMENT - R Code to Estimate Probability of Passing USP Dissolution Test
APR Sept/Oct 2023 - 57
APR Sept/Oct 2023 - 58
APR Sept/Oct 2023 - 59
APR Sept/Oct 2023 - 60
APR Sept/Oct 2023 - 61
APR Sept/Oct 2023 - FORMULATION AND DEVELOPMENT - Cloud Computing for Drug Discovery: The Time is Now
APR Sept/Oct 2023 - 63
APR Sept/Oct 2023 - 64
APR Sept/Oct 2023 - 65
APR Sept/Oct 2023 - 66
APR Sept/Oct 2023 - 67
APR Sept/Oct 2023 - CGT CIRCUIT - Navigating the Complex Testing Strategies for Viral Vector-based Gene Therapies
APR Sept/Oct 2023 - 69
APR Sept/Oct 2023 - MANUFACTURING - Simplifying Finished Product Manufacturer Site Transfer Variations
APR Sept/Oct 2023 - 71
APR Sept/Oct 2023 - 72
APR Sept/Oct 2023 - 73
APR Sept/Oct 2023 - FORMULATION AND DEVELOPMENT - Advancing Regulatory Compliance with Natural Language Processing
APR Sept/Oct 2023 - 75
APR Sept/Oct 2023 - 76
APR Sept/Oct 2023 - 77
APR Sept/Oct 2023 - DRUG DELIVERY - Finding a Greater Vantage Point for Creating Green Therapies
APR Sept/Oct 2023 - 79
APR Sept/Oct 2023 - 80
APR Sept/Oct 2023 - 81
APR Sept/Oct 2023 - WHITEPAPER - Microbial Testing for the Pharmaceutical Industry
APR Sept/Oct 2023 - 83
APR Sept/Oct 2023 - 84
APR Sept/Oct 2023 - 85
APR Sept/Oct 2023 - Facility Tour - Eurofins BioPharma Product Testing
APR Sept/Oct 2023 - 87
APR Sept/Oct 2023 - 88
APR Sept/Oct 2023 - ROUNDTABLE - Drug Delivery
APR Sept/Oct 2023 - 90
APR Sept/Oct 2023 - 91
APR Sept/Oct 2023 - MANUFACTURING - Accelerating Biologics R&D with Unified Software and Data Flows
APR Sept/Oct 2023 - 93
APR Sept/Oct 2023 - An Interview with Jason Downing, Senior Product Manager, TriLink BioTechnologies®
APR Sept/Oct 2023 - 95
APR Sept/Oct 2023 - FORMULATION AND DEVELOPMENT - The Role of Data in the Pharmaceutical Lifecycle
APR Sept/Oct 2023 - 97
APR Sept/Oct 2023 - 98
APR Sept/Oct 2023 - BIOPHARMACEUTICAL - Uniting Quality Expectations on Reinvigorated Biopharma Campuses
APR Sept/Oct 2023 - 100
APR Sept/Oct 2023 - 101
APR Sept/Oct 2023 - WHITEPAPER - VITAMIN C – Tableting with LUBRITAB® RBW Lubricant
APR Sept/Oct 2023 - 103
APR Sept/Oct 2023 - WHITEPAPER - Leveraging Analytical Technology Process for CMC
APR Sept/Oct 2023 - 105
APR Sept/Oct 2023 - 106
APR Sept/Oct 2023 - BIOPHARMACEUTICAL - Maximizing the Commercialization Potential of Cell and Gene Therapies
APR Sept/Oct 2023 - 108
APR Sept/Oct 2023 - 109
APR Sept/Oct 2023 - MICROBIOLOGY - Comments on Aseptic Process Simulation (APS) in the New EU GMP Annex 1
APR Sept/Oct 2023 - 111
APR Sept/Oct 2023 - 112
APR Sept/Oct 2023 - 113
APR Sept/Oct 2023 - VENDOR VIEWPOINT - Continuous & Intervention-Free Microbial Monitoring
APR Sept/Oct 2023 - 115
APR Sept/Oct 2023 - 116
APR Sept/Oct 2023 - 117
APR Sept/Oct 2023 - 118
APR Sept/Oct 2023 - 119
APR Sept/Oct 2023 - 120
APR Sept/Oct 2023 - Cover3
APR Sept/Oct 2023 - Cover4
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