LATITUDE Pharmaceuticals Inc.
9675 Businesspark Avenue
San Diego, CA 92131
T: (858) 546-0624
E: Info@latitudepharma.com
W:www.latitudepharma.com
LinkedIn: https://www.linkedin.com/company/latitude-pharmaceuticals

LATITUDE Pharmaceuticals: Your Drug Formulation Specialist

LATITUDE Pharmaceuticals is a client-focused CDMO with over 20 years of providing innovative drug formulation services and GMP manufacturing for early-phase clinical trials to the human and animal health industries. Founded in 2003, we have completed more than 1,200 client projects and have established a reputation for successfully formulating highly challenging compounds.

Formulation Development

LATITUDE’s formulation scientists are the foundation for our creative custom formulation development, reliability, transparency, rapid turnaround, and client satisfaction.  LATITUDE’s extensive experience and technical strengths in a wide range of dosage forms successfully address the most difficult formulation challenges including solubility, instability, bioavailability and in vivo adverse reactions. LATITUDE scientists have particular expertise in the formulation of complex injectables including nanoemulsions, liposomes, microspheres and nanoparticles.

Innovative Drug Delivery Platforms

LATITUDE has developed the following cutting-edge drug delivery platforms:

• ClearSol (Solubilization): A highly effective and safe solubilization technology that surpasses cyclodextrins in scope and concentration for a wide range of APIs, with all components being GRAS and FDA-approved for injection.
• PG Depot (Phospholipid Gel Depot): Designed for customizable, sustained release of subcutaneously or intramuscularly administered drugs over 1-7 days, with up to 20% drug loading as well as administration via fine needles.
• Nano-E (Nanoemulsion): A flexible, solubility-enhancing platform suitable for oral and injectable formulations, effective in minimizing vein irritation in injectables.
• ARTSS (Aqueous Room Temperature-Stable Solutions): LATITUDE’s platform for converting lyophilized powders or cold-stored solutions into RT-stable aqueous solutions.

GMP Manufacturing

In addition to providing materials for preclinical/IND-enabling studies, LATITUDE Pharmaceuticals manufactures and provides analytical testing for GMP-compliant clinical trial materials – we specialize in rapid delivery of Phase 1 and Phase 2 CTM. With a Quality Assurance System managed by an experienced and dedicated staff, LATITUDE can manufacture a variety of dosage forms including sterile injectable or ophthalmic drugs, as well as non-sterile oral or topical formulations, to support GLP toxicology studies or early-stage human clinical trials.  LATITUDE is particularly proficient in the manufacture of complex liquid formulations such as nanoemulsions, liposomes, nanoparticles and other controlled-release products.

Contact us for more information and to discuss how LATITUDE can meet your formulation or manufacturing needs.