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Collaborative, Licensing and Other Arrangements
9 Months Ended
Sep. 30, 2026
Research and Development [Abstract]  
Collaborative, Licensing and Other Arrangements Collaborative, Licensing and Other Arrangements
The Company enters into collaborative arrangements for the research and development, manufacture and/or commercialization of drug products and drug candidates. To date, these collaborative arrangements have included out-licenses of and options to out-license internally developed products and drug candidates to other parties, in-licenses of products and drug candidates from other parties, and profit- and cost-sharing arrangements. These arrangements may include non-refundable upfront payments, contingent obligations for potential development, regulatory and commercial performance milestone payments, cost-sharing and reimbursement arrangements, royalty payments, and profit sharing. For detailed descriptions of each arrangement, see the Company’s Annual Report.
For the three and nine months ended September 30, 2026 and 2025, the Company’s other revenue consisted primarily of royalty revenue from IMDELLTRA® sales outside of China under the Amgen collaboration agreement and revenue generated under the Novartis broad markets agreement.
The following table summarizes total other revenue recognized for the three and nine months ended September 30, 2026 and 2025:
Three Months EndedNine Months Ended
September 30,September 30,
2026202520262025
Other Revenue$$$$
Amgen royalty revenue25,744 12,169 62,864 26,721 
Novartis broad markets revenue6,869 4,115 17,088 10,957 
Other2,145 987 6,192 1,566 
Other Revenue34,758 17,271 86,144 39,244 
In-Licensing Arrangements - Commercial
Amgen
During the three and nine months ended September 30, 2026 and 2025, the Company recorded the following amounts related to its collaboration arrangement with Amgen. For a detailed description of the arrangement and related rights and obligations, see the Company’s Annual Report. The Company is still in the commercialization period for XGEVA®, KYPROLIS® and BLINCYTO® in China.
Amounts recorded related to the Company’s portion of the co-development funding on the pipeline assets for the three and nine months ended September 30, 2026 and 2025 were as follows:
Three Months EndedNine Months Ended
September 30,September 30,
2026202520262025
$$$$
BeOne’s portion of the development funding12,204 59,325 130,070 152,040 
Less: Amortization of research and development cost share liability6,182 29,275 64,345 74,844 
Research and development expense6,022 30,050 65,725 77,196 
The Company fulfilled its research and development cost share liability during the three months ended September 30, 2026. As of September 30, 2026 and December 31, 2025, the research and development cost share liability recorded in the Company’s balance sheet was as follows:
As of
September 30,December 31,
20262025
$$
Research and development cost share liability, current portion— 64,345 
Total research and development cost share liability— 64,345 
The total reimbursement paid under the commercial profit-sharing agreement for product sales is classified in the income statement for the three and nine months ended September 30, 2026 and 2025 as follows:
Three Months EndedNine Months Ended
September 30,September 30,
2026202520262025
$$$$
Cost of sales - product5,859 9,962 29,772 26,989 
Research and development(1,332)(371)(2,657)(2,480)
Selling, general and administrative(32,870)(24,546)(86,395)(73,531)
Total(28,343)(14,955)(59,280)(49,022)
The Company purchases commercial inventory from Amgen to distribute in China. Inventory purchases amounted to $177,997 and $433,707 for the three and nine months ended September 30, 2026, respectively, and $84,243 and $220,275 for the three and nine months ended September 30, 2025, respectively. Net amounts payable to Amgen was $146,707 and $79,097 as of September 30, 2026 and December 31, 2025, respectively.

In-Licensing Arrangements - Development
The Company has in-licensed the rights to develop, manufacture and, if approved, commercialize multiple development stage drug candidates globally or in specific territories. These arrangements typically include non-refundable upfront payments, contingent obligations for potential development, regulatory and commercial performance milestone payments, cost-sharing arrangements, royalty payments, and profit sharing.
Upfront and milestone payments incurred under these arrangements for the three and nine months ended September 30, 2026 and 2025 are set forth below. All upfront and development milestones were expensed to research and development expense. All regulatory and commercial milestones were capitalized as intangible assets and are being amortized over the remainder of the respective product patent or term of the commercialization agreements.
Three Months EndedNine Months Ended
September 30,September 30,
2026202520262025
Payments due to collaboration partnersClassification$$$$
Upfront paymentsResearch and development expense—191 20,518 691 
Development milestones incurredResearch and development expense757 — 4,070 — 
Regulatory and commercial milestone paymentsIntangible asset— — — 20,000 
Total757 191 24,588 20,691