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Innoviva Inc

Innoviva, Inc. is a biopharmaceutical company operating in the United States and internationally. Its royalty portfolio includes RELVAR/BREO ELLIPTA, a once-daily combination medicine of the LABA vilanterol and the inhaled corticosteroid fluticasone furoate, and ANORO ELLIPTA, a once-daily medicine combining the long-acting muscarinic antagonist umeclidinium bromide and a LABA. The company also markets GIAPREZA for increasing blood pressure in adults with septic or other distributive shock; XACDURO, a co-packaged intravenous treatment for hospital-acquired and ventilator-associated bacterial pneumonia caused by Acinetobacter; XERAVA for complicated intra-abdominal infections in adults; ZEVTERA, an advanced-generation cephalosporin antibiotic for Staphylococcus aureus bacteremia, right-sided endocarditis, acute bacterial skin and skin structure infections, and community-acquired bacterial pneumonia; and NUZOLVENCE for uncomplicated urogenital gonorrhea in adults and adolescents. It also develops bacteriophages for potential use in infectious and other serious diseases. The company has a strategic partnership with Sarissa Capital Management LP and a LABA Collaboration Agreement with Glaxo Group Limited to develop and commercialize once-daily products for chronic obstructive pulmonary disease and asthma. Formerly known as Theravance, Inc., it changed its name to Innoviva, Inc. in January 2016, was incorporated in 1996, and is headquartered in Burlingame, California.

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INVA

Innoviva Subsidiary Nortiva Bio Launches as Clinical-Stage Biopharma with LYNX Drug Delivery Platform

Innoviva announced that its wholly owned subsidiary Nortiva Bio has launched as a clinical-stage biopharmaceutical company focused on developing long-acting oral medicines using the proprietary LYNX drug delivery platform. Innoviva acquired the LYNX platform from Lyndra Therapeutics in 2025, and it is designed to transform daily pills into single-dose therapies lasting up to a month across multiple therapeutic areas. The platform is built on foundational science from the labs of Robert Langer and Gio Traverso at MIT and has undergone years of clinical validation, including a successful Phase 3 study.
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INVA

Innoviva Launches Nortiva Bio to Advance Long-Acting Oral Drug Platform

Innoviva has launched Nortiva Bio, a clinical-stage biopharmaceutical company focused on developing long-acting oral therapies using its proprietary LYNX drug delivery platform. The technology is designed to convert traditional daily oral medicines into extended-release treatments with potential dosing intervals of up to one month. Nortiva Bio operates as a wholly owned subsidiary of Innoviva following the acquisition of the LYNX platform from Lyndra Therapeutics in 2025. Separately, Innoviva Specialty Therapeutics, another subsidiary, announced an exclusive distribution and licensing agreement with Dr. Reddy's Laboratories for XACDURO in selected international markets, covering South and Central America, the Caribbean, Russia, and Commonwealth of Independent States countries. Under the deal, Dr. Reddy's will handle development, regulatory processes, and commercialization, while Innoviva Specialty Therapeutics retains rights outside the licensed regions and is eligible for upfront payments, milestone payments, and royalties.
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Biotech & Genomic Medicine

Innoviva Specialty Therapeutics Partners With Dr. Reddy’s to Expand XACDURO Access Internationally

Innoviva Specialty Therapeutics has entered an exclusive licensing and distribution agreement with Dr. Reddy’s Laboratories to bring XACDURO to South and Central America, the Caribbean, Russia, and the CIS region. The partnership targets carbapenem-resistant Acinetobacter infections, which exceed 70% in these areas. Dr. Reddy’s will handle development, regulatory approval, and commercialization within the territories, while Innoviva retains rights elsewhere and will receive an upfront payment, milestone payments, and tiered royalties on future net sales. XACDURO is FDA-approved for hospital-acquired and ventilator-associated bacterial pneumonia caused by Acinetobacter, a pathogen deemed a critical threat.
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