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BioWorld - Monday, March 23, 2026
Home » Topics » Deals and M&A

Deals and M&A
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Gold wireframe handshake

Masimo to buy Nanthealth’s connected care business, provides estimates for 2020 guidance

Jan. 14, 2020
By Liz Hollis
Irvine, Calif.-based Masimo Corp. has agreed to buy the connected care assets of Nanthealth Inc., of Culver City, Calif., for a $47.25 million up-front cash payment. In addition, Masimo provided estimates for its full-year 2020 financial guidance, saying product revenue will increase to $1.035 billion, which reflects reported growth of 10.6% to 10.9%. The transaction is expected to close in the first quarter of the year, subject to customary closing conditions. In addition, Masimo expects to fund the acquisition with existing cash on hand.
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Mundipharma to commercialize Samsung Bioepis’ biosimilars in Taiwan and Hong Kong

Jan. 14, 2020
By Jihyun Kim
HONG KONG – Global pharmaceutical company Mundipharma Pte Ltd. is gaining exclusive commercialization rights in Taiwan and Hong Kong to four biosimilar candidates from South Korean biopharma Samsung Bioepis Co. Ltd. targeting immunology and oncology.
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Allo’, allo’, allo’: Adaptimmune, Astellas enter potential $897.5M allogeneic stem cell therapy pact

Jan. 14, 2020
By Cormac Sheridan
Adaptimmune plc continued its bright start to the year by entering an alliance worth up to $897.5 million with Astellas Pharma Inc. to co-develop and co-commercialize stem cell-based allogeneic CAR T and T-cell receptor (TCR) cell therapies.
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Globe showing Asia-Pacific region

Mundipharma to commercialize Samsung Bioepis’ biosimilars in Taiwan and Hong Kong

Jan. 14, 2020
By Jihyun Kim
HONG KONG – Global pharmaceutical company Mundipharma Pte Ltd. is gaining exclusive commercialization rights in Taiwan and Hong Kong to four biosimilar candidates from South Korean biopharma Samsung Bioepis Co. Ltd. targeting immunology and oncology.
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Pfizer’s agreements with Biogen and Axsome lead day of deals

Jan. 13, 2020
By Lee Landenberger
Pfizer Inc. was a swinging door today as it sold its small molecule for treating patients with behavioral and neurological symptoms to Biogen Inc., while licensing reboxetine’s data and intellectual property and granting esreboxetine’s development and commercialization rights to Axsome Therapeutics Inc.
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Gennbio licenses in two immunosuppressants valued up to $164M from Genexine

Jan. 13, 2020
By Jihyun Kim
Gennbio Co. Ltd. has signed an agreement with fellow Korean biotech Genexine Inc. to in-license two immunosuppressant drug candidates called GX-P1 (PD-L1 hyfc) and BSF-110 (PD-L1-hyFc-1L10m).
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Gold chain link engraved with "partnership"
Up to $1.1B in milestones

Morphosys banks $750M up front plus $150M in stock sale as Incyte swoops in on tafasitamab

Jan. 13, 2020
By Cormac Sheridan
Ten days after its JAK1 inhibitor, itacitinib, failed a phase III trial in acute graft-vs.-host-disease (GVHD), Incyte Corp. has finalized a deal that could provide an alternative growth path. It is paying Morphosys AG $750 million up front, investing $150 million in its stock and is on the hook for up to $1.1 billion in milestones for a 50% interest in U.S. rights to the CD19-targeting antibody tafasitamab (MOR-208) and for 100% of the rights in all other territories.
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Morphosys banks $750M up front plus $150M in stock sale as Incyte swoops in on tafasitamab

Jan. 13, 2020
By Cormac Sheridan
1-10-sebacia.png

Sebacia names CEO, picks up Sienna assets

Jan. 10, 2020
By Liz Hollis
Duluth, Ga.-based Sebacia Inc., which is focused on dermatology and aesthetics, has introduced its new CEO and reported the acquisition of all assets related to Sienna Biopharmaceuticals Inc.'s silver photoparticle technology, which is being reviewed by the FDA for light hair removal.
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Lilly builds its dermatology pipeline with $1.1B Dermira acquisition

Jan. 10, 2020
By Lee Landenberger
Eli Lilly and Co.’s acquisition of Dermira Inc. for $1.1 billion in cash enlarges Lilly’s dermatology pipeline with the addition of lebrikizumab, a monoclonal antibody designed to bind IL-13 with high affinity, now in two phase III studies for treating moderate to severe atopic dermatitis (AD) in adolescent and adult patients, ages 12 and older.
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