Eikon $351M Series D, BridGene and Takeda Collab, BridgeBio Oncology to Go Public

Recent Funding:

Eikon Therapeutics (SF) Closes $351M Series D to Advance Pivotal-Stage Oncology Pipeline

Eikon raised $350.7M in a Series D financing, bringing its total private funding to over $1.1B. Investors include Lux Capital, T. Rowe Price, and UC Investments. Lead program EIK1001, a TLR7/8 co-agonist, is in Phase III for advanced melanoma, with additional PARP1 inhibitors and androgen receptor antagonists in early-stage development.

M&A, Deals, Partnerships

Eli Lilly Acquires Organovo’s (SD) Oral FXR Agonist for IBD in $10M Deal

Lilly acquired Organovo’s FXR program, including lead candidate FXR314, an oral small molecule in Phase 2/3 for inflammatory bowel disease (IBD), for up to $50M. Organovo receives $9M upfront, $1M after 15 months, and potential milestone payments. FXR agonists have faced regulatory challenges, but FXR314 may have applications in metabolic diseases and oncology.

BridGene Biosciences (SF) Secures $46M in Collaboration with Takeda for Immunology and Neurology Targets

Takeda has renewed its partnership with BridGene to develop small molecules targeting challenging immunology and neurology conditions, with up to $770 million in potential milestones. BridGene will leverage its IMTAC platform to identify and develop small molecules, with Takeda holding exclusive commercialization rights.

IPOs:

BridgeBio Oncology (SF) to Go Public via $450M SPAC Merger with Helix Acquisition Corp.

BridgeBio Oncology, a cancer-focused spinout from BridgeBio Pharma, will merge with SPAC Helix Acquisition Corp., securing ~$450M to advance its pipeline. The company has three oncology drugs in early-stage development, including two KRAS-targeting therapies and a PI3Ka-RAS inhibitor for solid tumors.

Other Interesting News:

Pliant Therapeutics (SF) Halts Phase 2b IPF Trial Due to Safety Concerns

Pliant discontinued the Phase 2b BEACON-IPF trial for bexotegrast in idiopathic pulmonary fibrosis (IPF) after safety concerns, despite early efficacy signals. The company will analyze data to determine future plans, including potential dose-ranging Phase 2b studies in pulmonary fibrosis and non-respiratory indications.