Pharma BD Deal Intelligence

Bristol-Myers Squibb Company / Century Therapeutics Inc.

2022 · Co-Development · $3.1B · Terminated

BMS paid Century Therapeutics $100M upfront plus a $50M equity stake against up to $3B for four iPSC-derived NK/T-cell programs, but terminated the collaboration without cause in December 2024, effective March 2025 — Century booked the remaining $109.2M as one-time revenue and pivoted CNTY-101 toward autoimmune disease.

Outcome grade pending — assessed 5 years post-close.

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The coverage arc

Jan 10, 2022 BioPharma Dive Bullish

Bristol Myers Squibb has signed a research deal worth up to $3 billion with Century Therapeutics, deepening its commitment to cell therapy as it works to…

Jan 10, 2022 STAT News Bullish

Bristol Myers Squibb has struck a deal worth as much as $3 billion with Century Therapeutics, a Philadelphia biotech developing cell therapies derived from…

May 15, 2025 SEC EDGAR (Century 10-Q Q1 2025) Bearish

Bristol-Myers Squibb notified the Company on December 12, 2024 that it would be terminating the Collaboration Agreement in its entirety without cause after the…

Source summaries from our enrichment pipeline; follow links for originals.

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BMS and Century Therapeutics entered a strategic collaboration to develop and commercialize up to four iPSC-derived allogeneic NK and T-cell therapy programs in hematologic malignancies and solid tumors. Century received $100M upfront plus a $50M equity investment, with up to $3B in additional payments plus royalties. UPDATE (terminated): On December 12, 2024 BMS notified Century that it would terminate the collaboration in its entirety, without cause, following an internal portfolio-prioritization review; the termination became effective March 12, 2025. Century recognized the remaining $109.2M deferred transaction price as one-time collaboration revenue in Q1 2025, with no further collaboration revenue expected. Century has since refocused lead asset CNTY-101 from oncology toward autoimmune disease (CALiPSO-1).

Key facts

Disease & market context

Hematologic Malignancies (Allogeneic Cell Therapy)

187K US cases/yr · $12.8B Global cell therapy oncology market 2023

Disease Overview

Hematologic malignancies — acute myeloid leukemia (AML), acute lymphoblastic leukemia (ALL), multiple myeloma, non-Hodgkin lymphoma (NHL), chronic lymphocytic leukemia (CLL), and Hodgkin lymphoma — collectively account for roughly 187,000 new U.S. cases and 60,000 deaths annually. Autologous CAR-T (Yescarta, Kymriah, Breyanzi, Tecartus, Carvykti, Abecma) has reset the treatment paradigm in B-cell lymphomas and multiple myeloma since 2017 with deep, durable responses but remains constrained by manufacturing variability, vein-to-vein time of 3-5 weeks, ICU-grade toxicity (CRS, ICANS), and access concentrated in academic centers. The strategic prize for allogeneic ('off-the-shelf') cell therapy is to compress vein-to-vein from weeks to days, expand to community oncology, and reduce cost — but to date, allogeneic donor T-cell platforms (Allogene, Atara, Precision BioSciences) have struggled with persistence and durability, and gene-edited iPSC-derived approaches like Century's are positioned as a third architectural path leveraging clonal master cell banks. BMS's existing CAR-T franchise (Breyanzi, Abecma) gives the deal direct strategic scaffolding.

Competitive Landscape

The allogeneic cell therapy competitive landscape is split across architectural choices, with each subclass facing distinct delivery and durability challenges. Donor-derived TALEN-edited T cells are pursued by Allogene Therapeutics (ALLO-501A anti-CD19 in EXPAND, ALLO-715 anti-BCMA in TRAVERSE), with persistence and durability the central technical challenge given lymphodepletion-related immune rejection of donor cells. NK-cell allogeneic platforms include Affimed and Artiva Biotherapeutics (cord-blood NK), Nkarta (gene-edited peripheral blood NK), and Fate Therapeutics' iPSC-derived NK cells (FT516, FT596) prior to Fate's 2023 strategic restructure that wound down most clinical NK programs. Gene-edited iPSC platforms — the Century approach — are also pursued by Sana Biotechnology (SC291 hypoimmune-edited CD19), Editas Medicine (EDIT-301/reni-cel in sickle/beta-thal), and BlueRock Therapeutics (Bayer subsidiary). Autologous CAR-T incumbents Yescarta (axicabtagene ciloleucel, Gilead/Kite), Breyanzi (lisocabtagene maraleucel, BMS), Kymriah (tisagenlecleucel, Novartis), Tecartus (brexucabtagene autoleucel, Gilead/Kite), Carvykti (ciltacabtagene autoleucel, J&J/Legend), and Abecma (idecabtagene vicleucel, BMS/2seventy bio) define commercial benchmarks at $400-500K list price. BMS's bet on Century is positioned as upside optionality and platform hedge to its existing autologous franchise rather than direct cannibalization, with the option to advance off-the-shelf next-gen successors as the autologous CAR-T market matures.

Deal timeline

Related deals — scored

DealYearValueOutcome
Bristol-Myers Squibb Company / Century Therapeutics Inc. (this deal)2022$3.1B
Bristol-Myers Squibb Company / Medarex Inc.2009$2.4B92
Bristol-Myers Squibb Company / Celgene Corporation2019$74.0B77
Bristol-Myers Squibb Company / MyoKardia Inc.2020$13.1B76
Bristol-Myers Squibb Company / Karuna Therapeutics2023$14.0B76
Bristol-Myers Squibb Company / Ono Pharmaceutical Co., Ltd.201176
Bristol-Myers Squibb Company / SystImmune Inc.2023$8.4B71

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