Serial Number
99036815
Owner
Franklin Biolabs, Inc.Attorney
Victoria D. SummerfieldFirst Use Date
Oct 1, 2024
Filing Date
Feb 11, 2025
FRANKLIN BIOLABS Trademark
Serial Number: 99036815
Trademark Classes
Owner Contact Info
Legal Representation
Correspondence Address
Victoria D Summerfield Troutman Pepper Locke
TROUTMAN PEPPER LOCKE
UNION TRUST BUILDING, 501 GRANT ST SUITE
Pittsburgh, PA 15219
United States
Trademark Details
Filing Date
February 11, 2025
Registration Date
Not Registered
First Use Anywhere
October 1, 2024
First Use in Commerce
October 1, 2024
Goods & Services
Custom manufacturing services for others in the fields of viral-based and non-viral vectors, pharmaceuticals, biologics, vaccines, biotechnological medical products, and gene and cell therapy preparations
Pharmaceutical research services; Pharmaceutical drug development and discovery services, namely, providing translational research tools and services, namely, providing scientific research in the field of screening, testing, sequencing, and analysis of DNA- and RNA-encoded genetic material for drug candidate development; cell and gene therapy product development services; Analytical services being scientific research services in the field of drug substance and drug product characterization which are for research use and in accordance with Good Manufacturing Practices (GMP); Preclinical services including pharmacology, pharmacokinetics, and toxicology in well established lab animal models; Scientific research and development and Good Laboratory Practices (GLP) services for bioanalytical testing including immunogenicity, biodistribution and shedding to support pre-clinical (animal) and clinical (human) studies; Chemistry, Manufacturing, and Controls (CMC) laboratory and stability testing for quality control purposes and analytical scientific advisory services in the fields of therapeutic drug evaluation and development, bioanalytical testing, immunogenicity testing, clinical studies, pre-clinical studies pharmacology, pharmacokinetics, and toxicology; Good Manufacturing Practices (GMP) laboratory and stability testing for quality control purposes and analytical scientific advisory services in the fields of therapeutic drug evaluation and development, bioanalytical testing, immunogenicity testing, clinical studies, pre-clinical studies pharmacology, pharmacokinetics, and toxicology; Providing laboratory research services for others in accordance with the Clinical Laboratory Improvement Amendments (CLIA) program to support the development of gene and cell therapy, biologics, vaccines, pharmaceuticals, and related biotechnological products; Research and development relating to production and analysis of viral-based vectors, pharmaceuticals, biologics, vaccines, biotechnological products, and gene and cell therapy preparations for use in medical research for others