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BioWorld - Sunday, April 19, 2026
Home » BMS

Articles Tagged with ''BMS''

Acquisition target

Tang Capital’s Concentra offers $465M cash buyout of Lianbio

Dec. 5, 2023
By Marian (YoonJee) Chu
Following its acquisition of Jounce Therapeutics Inc. for $95.6 million, Concentra Biosciences LLC lodged another proposal to acquire the U.S. and China biotech Lianbio Co. Ltd. The unsolicited and non-binding proposal filed Nov. 30 by San Diego-based Tang Capital Partners LP, Concentra’s parent firm, offered a 100% cash equity acquisition of the Shanghai- and Princeton, N.J.-based Lianbio at $4.30 per share, ringing up a deal worth around $465 million.
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Acquisition target

Tang Capital’s Concentra offers $465M cash buyout of Lianbio

Dec. 4, 2023
By Marian (YoonJee) Chu
Following its acquisition of Jounce Therapeutics Inc. for $95.6 million, Concentra Biosciences LLC lodged another proposal to acquire the U.S. and China biotech Lianbio Co. Ltd. The unsolicited and non-binding proposal filed Nov. 30 by San Diego-based Tang Capital Partners LP, Concentra’s parent firm, offered a 100% cash equity acquisition of the Shanghai- and Princeton, N.J.-based Lianbio at $4.30 per share, ringing up a deal worth around $465 million.
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BMS pays $350M up front for rights to Lianbio’s heart drug Camzyos in Asia

Oct. 31, 2023
By Marian (YoonJee) Chu
American pharma giant Bristol Myers Squibb Co. (BMS) will pick up the rights to Lianbio Co. Ltd.’s FDA-approved drug for obstructive hypertrophic cardiomyopath, Camzyos (mavacamten), in six Asian countries by paying $350 million up front and waiving some outstanding payments.
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BMS pays $350M up front for rights to Lianbio’s heart drug Camzyos in Asia

Oct. 25, 2023
By Marian (YoonJee) Chu
American pharma giant Bristol Myers Squibb Co. (BMS) will pick up the rights to Lianbio Co. Ltd.’s FDA-approved drug for obstructive hypertrophic cardiomyopath, Camzyos (mavacamten), in six Asian countries by paying $350 million up front and waiving some outstanding payments.
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PhRMA suit: IRA negotiations also a ‘taking’ from patients, providers

June 21, 2023
By Mari Serebrov
The floodgates have opened for challenges to the new U.S. drug price negotiation process laid out in the Inflation Reduction Act (IRA) that was narrowly passed last year.
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IRA pile-on expands with third challenge

June 20, 2023
By Mari Serebrov
Bristol Meyers Squibb Co. (BMS) joined the Inflation Reduction Act (IRA) pile-on June 16, filing a third constitutional challenge to the U.S. Medicare drug price negotiations mandated in the law that was narrowly passed last year on a partisan vote.
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Billion dollar deals blossom for Evotec and Bicycle

March 28, 2023
By Lee Landenberger
Two new deals, one a renewal that ups the ante on a previous agreement, have the potential to generate more than $1 billion each.
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Rx price increases intensify US scrutiny of industry practices

March 3, 2022
By Mari Serebrov
There’s nothing like beginning-of-the-year price increases to turn up the heat on the prescription drug pricing debate in the U.S. This year is no exception.  Citing a mean price increase of 5.1% on brand drugs in the first 25 days of 2022, 13 Democratic lawmakers, led by Sen. Elizabeth Warren (D-Mass.), wrote this week to Steven Ubl, president and CEO of the Pharmaceutical Research and Manufacturers of America, demanding an explanation for those hikes.
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CVR off the table: BMS’ liso-cel remains under FDA review in 2021

Jan. 4, 2021
By Jennifer Boggs
And just like that, it’s over. Bristol Myers Squibb Co. on Jan. 1 confirmed what many suspected, that FDA approval for lisocabtagene maraleucel (liso-cel) did not happen by the Dec. 31 deadline, thereby automatically terminating the contingent value rights (CVR) agreement issued as part of its acquisition of Celgene Inc.
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BMS’s deucravacitinib bests Otezla in psoriasis

Nov. 3, 2020
By Cormac Sheridan
Bristol Myers Squibb Co. reported that its first-in-class oral selective kinase 2 inhibitor, deucravacitinib (formerly BMS-986165), beat out Otezla (apremilast) in a head-to-head phase III trial in psoriasis.
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