LATITUDE Pharmaceuticals Inc.
9675 Businesspark Avenue
San Diego, CA 92131
Tel: 858-546-0624
Email: Info@latitudepharma.com

Website: www.latitudepharma.com    LinkedIn: https://www.linkedin.com/company/latitude-pharmaceuticals

LATITUDE Pharmaceuticals: Turning Complex Challenges into Clinical Reality

For over two decades, LATITUDE Pharmaceuticals Inc. has been helping biotechnology and pharmaceutical clients overcome complex formulation challenges and accelerate early-phase development for both human and animal health products.  As a client-centric CDMO, we bring innovation to every formulation and GMP manufacturing program — supported by more than 1,250 successful projects. LATITUDE has established a reputation for transforming difficult molecules into stable, bioavailable, and clinic-ready drug products.

Expertise in Complex Formulations

Our team of experienced formulation scientists are known for their creativity, technical rigor, and responsiveness. Their expertise spans a wide range of dosage forms and delivery routes, addressing issues such as poor solubility, instability, low bioavailability, and undesirable in vivo performance. LATITUDE is particularly recognized for its proficiency in complex injectables, including nanoemulsions, liposomes, microspheres, and nanoparticles, that demand both innovation and precision.

Innovative Drug Delivery Platforms

LATITUDE’s in-house technologies provide clients with unique solutions to accelerate development and improve the drug product profile:

  • ClearSol®: A solubilization platform for oral or injection formulations that outperforms cyclodextrins for a wide range of actives, using only GRAS and FDA-approved excipients.
  • PG Depot: A phospholipid gel depot enabling customizable, sustained release for subcutaneous or intramuscular delivery over 1–7 days, with up to 20% drug loading.
  • Nano-E: A versatile nanoemulsion technology enhancing solubility for oral and injectable products while minimizing vein irritation.
  • ARTSS: Converts lyophilized or cold-stored formulations into room-temperature-stable aqueous solutions, simplifying storage and distribution.

GMP Manufacturing & Analytical Support

Complementing our R&D strengths, LATITUDE provides GMP-compliant manufacturing and analytical testing for Phase 1 through non-pivotal Phase 3 clinical trial materials. The company’s quality system, experienced staff, and efficient project management enable rapid delivery of sterile injectables, ophthalmic drugs, oral solids / liquids, and topical drug products. LATITUDE excels at manufacturing complex liquids and controlled-release systems, ensuring consistency, compliance, and clinical readiness.

With its blend of scientific creativity, technical depth, and operational agility, LATITUDE Pharmaceuticals continues to help clients advance promising drug candidates from formulation concept to clinical reality.