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Home » Topics » Conferences » J.P. Morgan Healthcare Conference

J.P. Morgan Healthcare Conference
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Lilly’s ‘timely’ $2.5B Scorpion deal; GSK pays $1B up front for Idrx

Jan. 13, 2025
By Jennifer Boggs
Joining the dealmaking spree to kick off the 2025 J.P. Morgan Healthcare Conference, Eli Lilly and Co. announced it was picking up an early clinical-stage PI3Kα inhibitor program from Scorpion Therapeutics Inc. in a deal that could be worth up to $2.5 billion, while GSK plc is adding to its cancer pipeline with the acquisition of Idrx Inc. for $1 billion up front.
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Collage of businesspeople

Caplyta star shines as J&J takes Intra-Cellular in $14.6B deal

Jan. 13, 2025
By Randy Osborne
The J.P. Morgan (JPM) Healthcare Conference in San Francisco kicked off with a resounding bang as Johnson & Johnson (J&J) disclosed plans to acquire Intra-Cellular Therapies Inc. for $132 per share, which equates to an equity value of about $14.6 billion.
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JPM: Industry cutbacks ‘probably healthy overall’ as (better?) new year begins

Jan. 19, 2024
By Randy Osborne
Analysts from the hosting firm talked up their takeaways on biopharma from the J.P. Morgan (JPM) Healthcare Conference and looked ahead to 2024, anticipating a generally better year than those in the recent past.
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Hand holding 2024 with up arrows

Following JPM, 2024 outlook ranges from hopeful to cautious

Jan. 19, 2024
By Karen Carey
Setting the tone for the biopharma industry as it enters a new year, the J.P. Morgan Healthcare Conference (JPM) held each January has once again led to reflections, projections and earnest hopes for improving financial and M&A markets. Despite concerns over valuations, raising money and pricing issues, industry leaders are generally upbeat as the industry moves into 2024. JPM’s Sophie Jones, managing director of health care investment banking, noted in a Jan. 18 webinar sponsored by the Biotechnology Innovation Organization that the conference included more than 700 companies. “It’s morphing now into really the kickoff into everybody’s year.”
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Richard Lee, CEO, Lotte Biologics, at JPM24

Asia CDMO giants Wuxi and Samsung to grow production, ADC capacity

Jan. 16, 2024
By Marian (YoonJee) Chu
Major contract research development and manufacturing organizations (CDMO) out of Asia are announcing plans to ramp up production and antibody-drug conjugate (ADC) capabilities worldwide.
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PCV pipe(lines) robust; Merck at JPM with GSK, Vaxcyte in play

Jan. 12, 2024
By Randy Osborne
Merck & Co. Inc. CEO Robert Davis said the pneumococcal vaccines (PCVs) space is “an area where there is still a high unmet need, and what we have is a new vaccine specifically targeted to the adult population that addresses 83% of the residual disease. That's about 30% higher than anyone else that's out there.” Speaking Jan. 9 at the J.P. Morgan Healthcare Conference (JPM), Davis predicted that his firm “will take a majority share” of the market if approved. The Merck candidate, V-116, bears a PDUFA date with the U.S. FDA of June 17.
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JPM recap: Biopharma rising to postmarketing challenges in 2024

Jan. 12, 2024
By Jennifer Boggs
“This is a tough business. It’s never a straight line from start to success.” Those words, from Exelixis Inc. CEO Michael Morrissey, during a presentation at the J.P. Morgan Healthcare Conference (JPM), could easily sum up any aspect of the biopharma industry. But with more biopharma firms than ever having reached commercial status, along with the introduction of new therapeutic modalities into the health care market, many are finding the toughest part comes after regulatory approval, whether it’s navigating a competitive landscape, getting payers and physicians on board, or satisfying regulators’ stringent postmarketing requirements. As industry players and observers head home after a busy week in San Francisco, BioWorld offers a brief glimpse at a few firms taking on those post-approval challenges in 2024.
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DNA in drug capsules

The year of gene therapy? FDA’s Marks calls for solutions to regulatory, manufacturing challenges

Jan. 12, 2024
By Nuala Moran
The U.S. FDA is promising to make 2024 a “breakout” 12 months for gene therapies, with a number of initiatives to promote clinical development, approvals and uptake. “This is a great year to focus on gene therapy,” said Peter Marks, director of the Center for Biologics Evaluation and Research at the FDA. “I just want to focus on moving ahead gene therapy,” he told attendees of the J. P. Morgan Healthcare Conference on Jan. 8.
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New boss in FOS? Xenon featured at JPM; Biohaven also in play

Jan. 11, 2024
By Randy Osborne
Xenon Pharmaceuticals Inc. took to the stage this week at the J.P. Morgan Healthcare Conference to talk up its pipeline, including the phase III program testing XEN-1101 in focal-onset seizures (FOS), due to complete enrollment in the second half of this year. It’s an indication where such other players as Biohaven Ltd. are busy, too. Several million adults are afflicted with FOS in the U.S., with close to a half-million pediatric patients.
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Cancer cells

Making the circuit at JPM, Relay galvanized for big year ahead in PI3Ka, FGFR2

Jan. 10, 2024
By Randy Osborne
Among the firms updating progress at the J.P. Morgan Healthcare Conference (JPM) in San Francisco this week was Relay Therapeutics Inc., coming off a $30 million financing to boost its Dynamo platform and candidates.
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