Sunovion targets 22,000 psychiatrists with Latuda reps
Latuda hit pharmacy shelves in February, and reps will emphasize the drug's efficacy and positive cardiometabolic profile, according to slides presented by Mark Iwicki, president and COO, Sunovion, at a meeting in Tokyo on January 25. An additional team of 70 reps will target hospitals, and a “majority” of all reps “have previously sold at least 1 other atypical antipsychotic,” according to the slides. AbelsonTaylor has the professional AOR assignment.
Susan Adler, a Sunovion spokesperson, said patient support programs for Latuda are in place, and that materials for patients would be a component of the company's promotional efforts. TV spots will probably not be used, said Adler. “In general, atypical antipsychotic product [marketers] wouldn't focus on [televised] DTC ads,” she said.
Latuda was tested against olanzapine (Zyprexa) for weight change as part of Sunovion's PEARL study, and findings indicated that patients taking Latuda experienced an average change in weight of roughly 2.2 pounds for a 40 mg dosage, and 2.4 pounds for a 120 mg dosage; Latuda is currently available in 40 and 80 mg dosages, to be taken once daily. Olanzapine (15 mg) demonstrated an average weight change of 9.2 pounds in the PEARL study. Adler declined to speak about the drug's metabolic profile with respect to marketing plans.
Sunovion is testing Latuda for bipolar depression, and plans to submit an sNDA during the first half of 2012, according to a slide presentation given by Antony Loebel, EVP, clinical research and medical affairs, at the meeting in January. The company expects to submit Latuda for approval in Canada and China this year, and is currently analyzing phase III data in Japan.
In Europe, “active partnering discussions” are in progress, according to Loebel's slides. An estimated two million people have schizophrenia in the US, according to company data.