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May 26, 2017
While 84% Anticipate Prescribing Biosimilars in Next 3 Years—up from 70% 6 Months Earlier—Those Accepting Pharmacy-Level Substitution Drop From 28% to 17%
BOSTON, MA November 16, 2016— As the FDA approves more biosimilars—lower cost, similar yet not identical versions of already approved biologic drugs—a notably larger percentage of US physicians say they intend to prescribe them in the coming three years. However, fewer would allow pharmacy-level substation of these drugs for their patients than just six months ago, and they are weighting more factors into their choice of potentially prescribing biosimilars at all.
Data comes from a new biosimilars prescribing intentions tracking report developed by InCrowd, a provider of real-time market intelligence to the life sciences and healthcare firms.
The new data show that 84% of physicians across five subspecialties in which biologics prescribing is significant—dermatology, endocrinology, gastroenterology, oncology and rheumatology—surveyed in September 2016 said they expect to prescribe, assume they will prescribe, or look forward to prescribing more biosimilars in the next 3 years—up from 70% in February 2016. The figure reflects a decrease in those physicians who would only prescribe biosimilars if they were forced to do so, or there were specific patient conditions that warranted a move away from the originating biologic—from 26% in February to 16% in September.
However only 17% of total physicians surveyed in September said they would not prohibit biosimilars substitutions on their prescriptions for the originator biologic, down from 28% in February. Verbatims echoed their increased caution. “At this time I would not be amenable to switching a patient from a stable medication without significant data to prove complete compatibility,” said one rheumatologist. “I would wait and let other doctors experiment on their patients,” said an oncologist.”
In addition, among the top 10 most important factors in deciding to prescribe a biosimilar, physicians now are placing greater emphasis on thought leader opinions and professional organization guidelines—now at 55%, from 46% in February—as well as patient acceptance of biosimilars, up to 49% from 40%.
“Data reflect that during this time when biosimilars are of strong interest to insurers and health care systems for cost control, physicians are not rushing to issue a blank check for their substitution, and are keenly aware of their need to thoughtfully consider any such use,” said Diane Hayes, president and co-founder of InCrowd.
The September survey on US physician prescribing intentions with biosimilars also showed:
Wave 2 of InCrowd’s Biosimilars Research was captured data with InCrowd’s MicroTracker—a real-time market tracking solution that saves hours in design and fielding of data—and included responses from 150 US-based, triple-verified, board-certified physicians in specialties where biologics prescribing is significant—including 30 each in dermatology, endocrinology, gastroenterology, oncology, and rheumatology who have been in practice between 3 and 39 years. Respondents have personally treated patients with biologics therapies, and were at least somewhat familiar with biosimilars treatments. Physicians responded between September 21-22, 2016 to a six-minute microsurvey.
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