Pharma BD Deal Intelligence

Johnson & Johnson / Momenta Pharmaceuticals Inc.

2020 · Acquisition/Merger · $6.5B · Complete

J&J's $6.5 billion cash acquisition of Momenta paid off on a nine-year delay: nipocalimab won FDA approval as IMAAVY for generalized myasthenia gravis in April 2025, and by April 2026 the FDA had granted Priority Review for a second indication (warm autoimmune hemolytic anemia), turning a single pre-commercial antibody into a multi-indication franchise.

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The coverage arc

Aug 19, 2020 J&J Snaps Up Momenta Pharmaceuticals in $6.5 Billion All-Cash Deal - BioSpace Bullish

Johnson & Johnson will acquire Momenta Pharmaceuticals for $52.50 per share in cash, or approximately $6.5 billion, gaining full global rights to nipocalimab,…

Aug 19, 2020 Johnson & Johnson Press Release Bullish

Johnson & Johnson announced a definitive agreement to acquire all outstanding shares of Momenta Pharmaceuticals, Inc. for $52.50 per share in cash,…

Oct 01, 2020 J&J Completion Press Release Neutral

Johnson & Johnson today announced that it has completed its acquisition of Momenta Pharmaceuticals, Inc. through Vigor Sub, Inc., a wholly-owned subsidiary of…

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Johnson & Johnson acquired Momenta Pharmaceuticals for approximately $6.5 billion ($52.50 per share in cash) via tender offer and merger, completed October 1, 2020, gaining nipocalimab (M281), an anti-FcRn antibody targeting autoantibody-driven diseases. The acquisition thesis has since been validated: on April 30, 2025 the FDA approved nipocalimab as IMAAVY (nipocalimab-aahu) for generalized myasthenia gravis (gMG) in adult and pediatric patients aged 12 and older who are anti-AChR or anti-MuSK antibody positive -- the first and only FcRn blocker approved across both antibody subtypes, based on the Phase 3 Vivacity-MG3 study. J&J is pursuing label expansion: it submitted an sBLA for warm autoimmune hemolytic anemia (wAIHA) in February 2026 (ENERGY Phase 2/3), for which the FDA granted Priority Review on April 27, 2026 as the potential first-ever approved wAIHA therapy, and nipocalimab holds Fast Track designation in Sjogren's disease. The asset has moved from pre-commercial pipeline to an approved, multi-indication FcRn franchise.

Key facts

Disease & market context

Warm Autoimmune Hemolytic Anemia (wAIHA)

45K US cases/yr · $840M Global wAIHA Market (2024)

Disease Overview

wAIHA is the most common form (60-70%) of autoimmune hemolytic anemia. Treatment shifting from corticosteroids and rituximab toward targeted therapies.

Competitive Landscape

Sanofi (rilzabrutinib, BTK) Phase 2 for wAIHA. Annexon (ANX005, C1q) and FcRn programs in development. Market projected >15% CAGR.

Hemolytic Disease of the Fetus and Newborn (HDFN)

4K US cases/yr · $500M Estimated Global HDFN Treatment Market

Disease Overview

HDFN occurs when maternal antibodies attack fetal red blood cells. FcRn inhibitors like nipocalimab could be transformative by reducing pathogenic maternal IgG transfer.

Treatment Landscape

Current management limited to intrauterine transfusion, phototherapy, and exchange transfusion. J&J's nipocalimab is in Phase 3 (UNITY) for HDFN prevention, potentially the first drug approved for this indication.

Deal timeline

Related deals — scored

DealYearValueOutcome
Johnson & Johnson / Momenta Pharmaceuticals Inc. (this deal)2020$6.5B72
Johnson & Johnson / Legend Biotech Corporation2017$9.0B96
Johnson & Johnson / Centocor Inc.1999$4.9B92
Johnson & Johnson / Cougar Biotechnology, Inc.2009$970M91
Johnson & Johnson / Actelion Ltd2017$30.0B90
Johnson & Johnson / Aragon Pharmaceuticals Inc.2013$1.0B89
Johnson & Johnson / Legend Biotech Corporation2017$350M83

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