VIVUS LLC
VIVUS is dedicated to addressing the therapeutic needs of patients with serious medical conditions and life-limiting diseases through clinical development and commercialization expertise. The company focuses on developing high-potential molecules into proprietary products to improve patient quality of life, provide new treatment options for healthcare providers, and create value for shareholders.
Industries
Nr. of Employees
medium (51-250)
VIVUS LLC
900 E. Hamilton Avenue, Suite 550, Campbell, CA 95008, USA
Patents
Orally disintegrating dosage form for administration of avanafil, and associated methods of manufacture and use
US-10028916-B2
View Details
Orally disintegrating dosage form for administration of avanafil, and associated methods of manufacture and use
US-10028916-B2
View DetailsProducts
Pancreatic enzyme replacement therapy (marketed product)
Oral pancreatic enzyme replacement formulation used to manage exocrine pancreatic insufficiency by providing digestive enzymes to aid nutrient absorption.
Oral weight management medication (marketed product class)
Once-daily oral medication for weight management used in adults and select pediatric populations as part of a comprehensive weight management program.
Pancreatic enzyme replacement therapy (marketed product)
Oral pancreatic enzyme replacement formulation used to manage exocrine pancreatic insufficiency by providing digestive enzymes to aid nutrient absorption.
Oral weight management medication (marketed product class)
Once-daily oral medication for weight management used in adults and select pediatric populations as part of a comprehensive weight management program.
Services
Telephone and email medical information service for healthcare professionals and patients, and contact channels for adverse event and product complaint reporting.
Point of contact for investigator-initiated clinical trial requests and collaboration inquiries (subject to current acceptance policies).
Regional commercialization activities including launch planning, market access, and distribution management across multiple geographies.
Implementation and maintenance of a written code of conduct, compliance officer oversight, employee training, auditing and monitoring programs.
Collaborative programs integrating medication with telehealth and digital lifestyle interventions to support patient treatment pathways.
Telephone and email medical information service for healthcare professionals and patients, and contact channels for adverse event and product complaint reporting.
Point of contact for investigator-initiated clinical trial requests and collaboration inquiries (subject to current acceptance policies).
Regional commercialization activities including launch planning, market access, and distribution management across multiple geographies.
Implementation and maintenance of a written code of conduct, compliance officer oversight, employee training, auditing and monitoring programs.
Collaborative programs integrating medication with telehealth and digital lifestyle interventions to support patient treatment pathways.
Expertise Areas
- Clinical trial management
- Regulatory compliance and submissions
- Chemistry, Manufacturing and Control (CMC)
- Quality assurance and supplier auditing
Key Technologies
- Clinical trial design and management
- Regulatory filing and lifecycle management
- CMC and formulation/process development
- Quality management and supplier audit programs