In Pfenex’s fourth-quarter 2017 investor call, Evert Schimmelpennink, CEO, president, secretary, and director, hinted that Pfenex may be ready to resume work on 2 biosimilar candidates whose programs had been on hiatus.
In Pfenex’s fourth-quarter 2017 investor call this month, Evert Schimmelpennink, CEO, president, secretary, and director, hinted that Pfenex may be ready to resume work on 2 biosimilar candidates whose programs had been on hiatus.
Previously, in its 2017 third-quarter call held in November 2017, Pfenex announced the company’s “decision to pause development activities” for PF582, a ranibizumab biosimilar referencing Lucentis, and PF529, a pegfilgrastim biosimilar referencing Neulasta, after a strategic review of both costs and development timelines for the drugs.
In this month’s call, Schimmelpennink said, “We continue to believe that the most prudent path for the development is a collaboration with a strategic development partner. As that business development process continues, we continue to seek partners with whom we would advance those programs.” Halting development of the 2 programs lowered research and development costs to $7.2 million in the fourth quarter of 2017 compared with $10.7 million in the same period in 2016, said Schimmelpennink.
Pfenex previously partnered with Hospira on the ranibizumab biosimilar candidate, but after Pfizer acquired Hospira in 2016, Pfizer terminated the collaboration.
Pfenex did not address its progress on the third biosimilar its pipeline, a pegaspargase candidate referencing Oncaspar. The company’s lead products include PF708, a “therapeutic equivalent candidate” to teriparatide (Forteo) for the treatment of osteoporosis, and 2 novel anthrax vaccine candidates, Px563L and RPA563, which it is developing through a contract with the US government.
In addition, the company continues to develop hematology and oncology products in collaboration with Jazz Pharmaceuticals. Under Pfenex’s agreement with Jazz, Pfenex received upfront and option payment totaling $15 million, and may be eligible to receive payments of up to $166 million based on achievements of certain development, regulatory, and sales milestones.
The Top 5 Most-Read Gastroenterology Articles of 2024
December 21st 2024The top gastroenterology biosimilar news from 2024 highlight fluctuations in the adalimumab biosimilar market throughout the year, while FDA and European approvals for ustekinumab biosimilars are set to improve access and reduce costs for patients with Crohn disease and ulcerative colitis.
Biosimilars Gastroenterology Roundup for November 2024—Podcast Edition
December 1st 2024On this episode of Not So Different, we discuss market changes in the adalimumab space; calls for PBM transparency and biosimilar access reforms grew; new data for biosimilars in gastroenterology conditions; and all the takeaways from this year's Global Biosimilars Week.
Biosimilars Development Roundup for October 2024—Podcast Edition
November 3rd 2024On this episode of Not So Different, we discuss the GRx+Biosims conference, which included discussions on data transparency, artificial intelligence (AI), and collaboration to enhance the global supply chain for biosimilars and generic drugs, as well as the evolving requirements for biosimilar devices.
13 Strategies to Avoid the Nocebo Effect During Biosimilar Switching
December 18th 2024A systematic review identified 13 strategies, including patient and provider education, empathetic communication, and shared decision-making, to mitigate the nocebo effect in biosimilar switching, emphasizing the need for a multifaceted approach to improve patient perceptions and therapeutic outcomes.