PMID- 33410093 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20210619 IS - 2509-4254 (Electronic) IS - 2509-4262 (Print) IS - 2509-4262 (Linking) VI - 5 IP - 2 DP - 2021 Jun TI - Understanding Patients' Willingness to Pay for Biphasic Insulin Aspart 30/70 in a Pen Device for Type 2 Diabetes Treatment in an Out-of-Pocket Payment Market. PG - 261-273 LID - 10.1007/s41669-020-00246-3 [doi] AB - OBJECTIVE: Our objective was to investigate willingness to pay (WTP) for biphasic insulin aspart 30/70 (BIAsp 30) in patients with type 2 diabetes mellitus (T2DM) in India. METHODS: A multicenter, prospective, non-interventional, preference study was conducted that assessed WTP for BIAsp 30 in an insulin pen (FlexPen((R)) or Penfill((R)) device) in patients in India with T2DM previously treated with biphasic human insulin (BHI) in vials and believed to be able to pay for treatment. The primary endpoint was the proportion of patients willing to continue to pay for BIAsp 30 after 12 weeks' treatment. Secondary endpoints included the change from baseline in treatment and device satisfaction and patient preferences for treatment attributes as assessed by a nested discrete-choice experiment. RESULTS: Overall, 54.9% (n = 277/505) of participants were male; the mean age was 56.4 years; diabetes duration was 10.9 years; 63.8% had a body mass index >/= 25 kg/m(2); > 75% had an annual household income > 150,000 Indian rupees (INR). After 12 weeks' treatment, 96.4% of patients were willing to pay for BIAsp 30. Mean treatment and device satisfaction significantly improved from baseline (p < 0.0001). Patients were willing to pay INR3576 (95% confidence interval [CI] 2755-4398) for improved glycemic control, INR688 (95% CI 383-994) for a device upgrade (vial/syringe to an insulin pen), or INR327 (95% CI 95-560) to avoid major hypoglycemia. Patients would need to be compensated INR44 (95% CI 56-32) per minor hypoglycemic event. CONCLUSIONS: In India, patients with T2DM previously treated with BHI were willing to pay for BIAsp 30 in an insulin pen. Furthermore, treatment and device satisfaction improved after this therapeutic switch. TRIAL REGISTRATION: ClinicalTrials.gov: NCT03374774. FAU - Murthy, Sreenivasa AU - Murthy S AD - LifeCare Hospital and Research Centre, Bangalore, Karnataka, India. drsreenivasamurthy@gmail.com. FAU - Aneja, Pankaj AU - Aneja P AD - Max Super Speciality Hospital, Shalimar Bagh, New Delhi, India. FAU - Asirvatham, Arthur Joseph AU - Asirvatham AJ AD - Arthur Asirvatham Hospital, Madurai, Tamil Nadu, India. FAU - Husemoen, Lise Lotte N AU - Husemoen LLN AD - Novo Nordisk A/S, Soborg, Denmark. FAU - Rhee, Nicolai A AU - Rhee NA AD - Novo Nordisk Health Care AG, Zurich, Switzerland. FAU - Kesavadev, Jothydev AU - Kesavadev J AD - Jothydev's Diabetes Research Center, Trivandrum, Kerala, India. LA - eng SI - ClinicalTrials.gov/NCT03374774 PT - Journal Article DEP - 20210106 PL - Switzerland TA - Pharmacoecon Open JT - PharmacoEconomics - open JID - 101700780 PMC - PMC8160041 COIS- NAR and LLNH are employees of the sponsor (at Novo Nordisk Health Care AG) and own shares in the company. JK is in the Speaker's bureau for Novo Nordisk. SM, PA, and AJA have no conflicts of interest that are directly relevant to the content of this article. EDAT- 2021/01/08 06:00 MHDA- 2021/01/08 06:01 PMCR- 2021/01/06 CRDT- 2021/01/07 06:14 PHST- 2020/12/10 00:00 [accepted] PHST- 2021/01/08 06:00 [pubmed] PHST- 2021/01/08 06:01 [medline] PHST- 2021/01/07 06:14 [entrez] PHST- 2021/01/06 00:00 [pmc-release] AID - 10.1007/s41669-020-00246-3 [pii] AID - 246 [pii] AID - 10.1007/s41669-020-00246-3 [doi] PST - ppublish SO - Pharmacoecon Open. 2021 Jun;5(2):261-273. doi: 10.1007/s41669-020-00246-3. Epub 2021 Jan 6.