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.”
From Amjevita to Zarxio: A Decade of US Biosimilar Approvals
March 6th 2025Since the FDA’s groundbreaking approval of Zarxio in 2015, the US biosimilars market has surged to 67 approvals across 18 originators—though the journey has been anything but smooth, with adoption facing hurdles along the way.
How AI Can Help Address Cost-Related Nonadherence to Biologic, Biosimilar Treatment
March 9th 2025Despite saving billions, biosimilars still account for only a small share of the biologics market—what's standing in the way of broader adoption and how can artificial intelligence (AI) help change that?
Will the FTC Be More PBM-Friendly Under a Second Trump Administration?
February 23rd 2025On this episode of Not So Different, we explore the Federal Trade Commission’s (FTC) second interim report on pharmacy benefit managers (PBMs) with Joe Wisniewski from Turquoise Health, discussing key issues like preferential reimbursement, drug pricing transparency, biosimilars, shifting regulations, and how a second Trump administration could reshape PBM practices.
The Banking of Biosimilars: Insights From a Leading Health Economist
February 4th 2025Biosimilars have the potential to reduce health care costs and expand patient access, but economic and policy barriers affect adoption, explored James D. Chambers, PhD, MPharm, MSc, associate professor at the Tufts Medical Center Institute for Clinical Research and Health Policy Studies, in an interview.