Coherus BioSciences has announced that it plans to raise up to $150 million in a 2-tranche private placement deal with Temasek.
Coherus BioSciences has announced that it plans to raise up to $150 million in a 2-tranche private placement deal with Temasek.
The first tranche of $75 million consists of 6,556,116 shares of common stock, issued at an offering price of $11.44 per share. The Singapore-based investment company plans to issue the second tranche after the FDA grants approval to CHS-1701, Coherus’ pegfilgrastim biosimilar (referenced on Amgen’s Neulasta).
Coherus says that it will use the funding for the development and eventual launch of CHS-1701. It will also dedicate some of the money to developing and registering CHS-1420 (an adalimumab biosimilar referenced on Humira) and to developing CHS-3351 (a ranibizumab biosimilar referenced on Lucentis).
“We are very pleased to have the support of a significant investor of Temasek’s stature and reputation as we continue to progress CHS-1701 and the rest of our pipeline,” Coherus CEO Denny Lanfear said. “We are gratified to have Temasek as a shareholder as we advance our efforts to bring biosimilar competition to the market, delivering cost savings for the healthcare system and increasing access to essential biologics for patients.”
The investment windfall is welcome news for the biosimilar developer, which restructured its business and terminated 30% of its workforce in July after the FDA issued a complete response letter for CHS-1701 in June. Despite the fact that it is not yet clear when Coherus will be able to resubmit a new application for the drug, the biosimilar has been the subject of costly Biologics Price Competition and Innovation Act (BPCIA) litigation since 2016.
In July, Coherus sought a stay of discovery in the case, saying that it needed to preserve its limited resources. Amgen’s answering brief argued that Coherus should be well aware of the costs that come with resolving patent disputes through litigation, and that “Whatever may have led to Coherus’s alleged financial hardship…it does not justify delaying discovery of information relevant to prepare this case for trial.”
Coherus, in its own reply brief filed last week, invoked both the BPCIA and its own need to preserve its financial resources, saying that “The BPICA does not require wasting money on discovery pending dispositive motions.”
Eye on Pharma: Korean Drugmakers’ Impact in Europe; New Denosumab, Eculizumab Deals
January 11th 2025Korean drugmakers hold over 50% market share in the 6 best-selling biosimilar markets, 2 companies sign exclusive licensing partnership for a denosumab biosimilar, and 2 others join forces for an eculizumab biosimilar.
Biosimilars in America: Overcoming Barriers and Maximizing Impact
July 21st 2024Join us as we explore the complexities of the US biosimilars market, discussing legislative influences, payer and provider adoption factors, and strategies to overcome industry challenges with expert insights from Kyle Noonan, PharmD, MS, value & access strategy manager at Cencora.
Commercial Payer Coverage of Biosimilars: Market Share, Pricing, and Policy Shifts
December 4th 2024Researchers observe significant shifts in payer preferences for originator vs biosimilar products from 2017 to 2022, revealing growing payer interest in multiple product options, alongside the increasing market share of biosimilars, which contributed to notable reductions in both average sales prices and wholesale acquisition costs.
Exploring the Biosimilar Horizon: Julie Reed's Predictions for 2024
February 18th 2024On this episode of Not So Different, Julie Reed, executive director of the Biosimilars Forum, returns to discuss her predictions for the biosimilar industry for 2024 and beyond as well as the impact that the Forum's 4 new members will have on the organization's mission.
Overcoming Challenges to Improve Access and Reduce Costs
November 12th 2024Biosimilars hold the potential to dramatically lower health care costs and improve access to life-changing treatments, but realizing this potential will require urgent policy reforms, market competition, and better education for both providers and patients.