Marina Biotech signed an agreement with Windlas Healthcare Limited to manufacture IT-102 fixed-dose combination bi-layer tablets.

Marina Biotech (OTCQB:MRNA) signed an agreement with Windlas Healthcare to manufacture IT-102 fixed-dose combination bi-layer tablets.
As quoted in the press release:

“This agreement marks the culmination of an in-depth due diligence and qualification process, during which we evaluated dozens of manufacturers, and Windlas came out ahead,” stated Joseph Ramelli, CEO of Marina Biotech. “The manufacturing of the FDC bi-layer tablets requires additional equipment and expertise that Windlas possesses. Now with this agreement in place we are positioned to move into a pivotal phase 3 clinical study by the first quarter of 2018.”
Marina Biotech’s IT-102, a celecoxib and lisinorpril FDC, is being developed for the combined treatment of arthritis and hypertension. The preference for and improved compliance with a single tablet makes the proposed FDC formulation a very useful drug for treatment of 2 common conditions with increasing frequency in the aging population. Additionally, the combination of lisinopril with celecoxib may reduce the incidence of cardiovascular adverse events and edema associated with celecoxib treatment, potentially making it a preferred treatment for pain. IT-102 will be further developed for treatment of familial adenomatous polyposis (FAP).
Windlass Healthcare Limited (WHC) corporate headquarters is in Gurgaon, India. The company was established in 2008 in Dehradun, and the manufacturing facilities are designed as per the US Food and Drug Administration (US FDA), and European Union current Good Manufacturing Practices (EU cGMP) standards. The manufacturing plant has received approval from USFDA.
About Marina Biotech
Marina Biotech is a biotechnology company focused on the development and commercialization of innovative therapeutics for disease intersections of arthritis, hypertension, and cancer. Our pipeline includes combination therapies of oligonucleotide-based therapeutics and small molecules. The Marina Biotech pipeline currently includes a clinical program in Familial Adenomatous Polyposis (a precancerous syndrome). By its merger with IthenaPharma, Marina Biotech recently acquired IT-102/IT-103 – next generation celecoxib — which will be developed together with CEQ508 as a therapeutic enhancer for therapies against FAP and CRC. IT-102/IT-103 are also being developed for the treatment of combined arthritis/ hypertension and treatment of pain requiring high dose of celecoxib. Additional information about Marina Biotech is available at

Click here to read the full press release.


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