The collaboration brings together Sandoz expertise in launching and commercializing treatments with Pear's leading experience in digital therapeutics design and implementation.
Sandoz and Pear will work together to bring reSET to patients with Substance Use Disorder and, if cleared by FDA, reSET-O to patients with Opioid Use Disorder who are currently receiving buprenorphine, to better address the full burden of their illnesses.
Pear's flagship digital therapeutic, reSET, was cleared by the FDA in September 2017 to help treat Substance Use Disorder.
Sandoz CEO Richard Francis said: "The opioid crisis is taking a devastating and growing toll on our communities and we all have a role to play in helping find solutions that work for patients, families and communities.
"Our agreement with Pear and its expertise in developing prescription digital therapeutics fits with our strategy to be a part of the solution to the issues plaguing people battling addiction, including opioids."
Pear's prescription digital therapeutics aim to be designed to deliver clinically proven treatments, such as cognitive behavioral therapy, to patients through mobile and desktop applications.
Once cleared by FDA, these digital therapeutics may be prescribed as monotherapies or alongside drug therapies and have the potential to be developed to treat a range of diseases.
Substance Use Disorder (SUD) is a chronic, relapsing disease caused by the recurrent use of alcohol or drugs – or both.
For people with SUD, treatment has typically meant resource intensive face-to-face interactions in a specialized setting, and inconsistent quality in treatment and limited accessibility has led to poor treatment outcomes, including low rates of abstinence and high dropout rates.
This collaboration is part of the Sandoz and Novartis strategic effort to work with innovative digital health leaders to drive the next wave of medical innovation.
Sandoz and Novartis are collaborating to develop technologies to monitor patient data in real-time, detect day-to-day behavioral and biological changes in condition, improve patient adherence, and ultimately enhance treatment outcomes by helping patients to better understand and control their own healthcare.
Pear is a leader in developing prescription digital therapeutics, developing the first FDA-cleared mobile medical application with both a safety and efficacy label to help treat patients with Substance Use Disorder in September 2017. Novartis invested in Pear's Series A and in its Series B rounds of financing.
Source: Company Press Release.