RegulatoryJ&J Shells Out $3B to Acquire Halda, Expanding Cancer...

J&J Shells Out $3B to Acquire Halda, Expanding Cancer Portfolio

-

A Strategic Move in Oncology

Johnson & Johnson is spending just over $3 billion in cash to purchase Halda Therapeutics, aiming to strengthen its oncology portfolio with a slate of oral solid tumor treatments.

Through the deal, J&J will pick up Halda’s pipeline of oral cancer therapies, according to Monday’s announcement. The centerpiece is HLD-0915, a once-daily prostate cancer drug that received the FDA fast track status in August.

Promising Clinical Results

Phase I/II results released in late 2024 showed promising early anti-tumor activity, including reductions in prostate cancer biomarkers and partial responses in all five evaluable patients. Halda is continuing to run its Phase I/II study in metastatic, castration-resistant prostate cancer (mCRPC).

Jennifer Taubert, EVP of Innovative Medicine at J&J, said in a statement that the acquisition bolsters the company’s already robust cancer portfolio by adding a promising prostate cancer program and a platform that could be applied to multiple cancers and other diseases, creating potential drivers of growth over the medium and long term.

Future Growth and Ambitions

During a second-quarter earnings call in July, CEO Joaquin Duato set an ambitious goal for Johnson & Johnson: to generate $50 billion in oncology sales by 2030.

Innovative RIPTAC Platform

Contributing to that ambition, Halda brings a discovery platform known as Regulated Induced Proximity Targeting Chimera (RIPTAC). Using this approach, the company designs paired ligands that bind two different proteins at once – one found mainly on tumor cells and another that performs an essential cellular function. By bringing these together, the drugs are intended to selectively kill cancer cells while minimizing damage to healthy tissue.

Halda classifies all of its candidates as RIPTACs. Beyond HLD-0915 in prostate cancer, its pipeline includes a breast cancer program aimed at hormone receptor–positive (HR+) tumors, a candidate being evaluated in lung cancer and additional early-stage oncology therapies that have not yet been disclosed in detail.

Rapid Payoff for a Young Company

For Halda, the buyout marks a rapid payoff for a relatively young company. Founded in 2019 out of the lab of Yale chemist Craig Crews, Halda quickly attracted investor interest, culminating in a second Series B round of $126 million to advance HLD-0915 and an unnamed breast cancer candidate through development.

J&J’s Broader Strategy

From Johnson & Johnson’s perspective, Halda is its second major acquisition of the year, following the $14.6 billion takeover of neuropsychiatry-focused Intra-Cellular Therapies in January, which is still the largest pharma M&A deal announced so far in 2025. At the time, J&J signaled that the remainder of 2025 would likely be relatively subdued on the business development front.

J&J and Halda expect the acquisition to wrap up in the coming months, pending antitrust approval and the fulfillment of other customary closing conditions, according to the companies’ announcement. Johnson & Johnson added that it plans to share more details on the transaction during its fourth-quarter earnings update in early 2026.

e8ca33a26f7037921e92de08cb2a519d8f9a37c9966383abf07edbf18b55cb25?s=150&d=mp&r=g
+ posts

Latest news

Artios Pharma Raises $115 Million to Advance DDR-Focused Oncology Pipeline

Expanding Clinical Development with New Funding Artios Pharma has secured $115 million in an oversubscribed series D financing round to...

CHMP Issues Positive Opinion for Sanofi Teizeild to Delay Progression to Stage 3 Type 1 Diabetes

A Groundbreaking Recommendation for T1D Intervention The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency...

Neurocrine’s Depression Drug Encounters Surprising Phase II Failure

Neurocrine Biosciences has hit a roadblock with its experimental oral therapy NBI-1070770, commonly referred to as ‘770, after the...

Must read

Surrounded by controversy, FDA approves Biogen’s Alzheimer’s drug Aduhelm

In the middle of the debate about the Alzheimer’s drug approval, the United States FDA has authorized Aduhelm

You might also likeRELATED
Recommended to you