Entry Into a Material Definitive Agreement

On July 28, 2022, Apellis Pharmaceuticals, Inc. (the "Company") reported that entered into separate, privately negotiated exchange agreements (the "Exchange Agreements") with certain holders of its 3.500% Convertible Senior Notes due 2026 (the "Notes") (Filing, 8-K, Apellis Pharmaceuticals, JUL 28, 2022, View Source [SID1234617323]). Under the terms of the Exchange Agreements, the holders have agreed to exchange with the Company approximately $22.5 million in aggregate principal amount of Notes held by them for (i) 456,128 shares of the Company’s common stock, which is equal to 20.2724 shares per $1,000 principal amount of Notes exchanged plus (ii) an additional number of shares of the Company’s common stock per $1,000 principal amount of Notes exchanged equal to the quotient of (a) $591.91 divided by (b) the average of the daily volume-weighted average prices of the Company’s common stock over the three consecutive trading days commencing on July 29, 2022 (collectively, the "Shares"). These exchange transactions are expected to close on August 4, 2022, subject to the satisfaction of customary closing conditions.

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Entry into a Definitive Material Agreement

On July 28, 2022, Radius Health, Inc. ("Radius") and Teijin Pharma Limited ("Teijin") reported that it entered into an Amendment to License and Development Agreement ("Amendment") to the License and Development Agreement ("LDA") entered into between Radius and Teijin on July 13, 2017 (Filing, 8-K, Radius, JUL 28, 2022, View Source [SID1234617277]).

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The LDA contemplates the commercialization of the active pharmaceutical ingredient abaloparatide for subcutaneous injection ("abaloparatide-SC") for the treatment of osteoporosis and included a joint commercialization opportunity between Teijin and Radius. Under the LDA, Radius grants Teijin a license to Radius intellectual property related to abaloparatide-SC in exchange for a royalty on net sales of abaloparatide-SC in Japan.

The LDA has been amended by the Amendment to remove references to the joint commercialization opportunity. The LDA has also been amended to waive the royalty on net sales of any abaloparatide-SC purchased by Teijin through a Commercial Supply Agreement ("CSA") entered into between Teijin and Radius concurrently with the Amendment. The Amendment does not have any impact on royalties owed on sales of abaloparatide-SC not purchased through the CSA, and accordingly, for any abaloparatide-SC sold by Teijin but not purchased through the CSA, royalty payments will be owed by Teijin to Radius under the LDA in consideration for the license granted by Radius to Teijin thereunder.

The Amendment also provides that the LDA may be terminated by either party due to a material breach of the CSA by the other party.

Under the CSA, Radius will supply to Teijin, and Teijin will purchase from Radius, a finished product comprising a cartridge filled with abaloparatide-SC ("Drug Product").

Specifically, Radius will purchase, for Teijin, the abaloparatide-SC from a material supplier and then have a commercial supplier fill the cartridges with abaloparatide-SC and supply final Drug Product for commercialization and distribution by Teijin in Japan. As consideration, Radius will receive an annual fee and a per-unit supply price for all Drug Product purchased by Teijin through Radius under the CSA. Any other costs borne by Radius for the purchase of abaloparatide-SC or manufacture of the Drug Product will be reimbursed by Teijin.

Radius has also agreed under the CSA, in the event of any breach of the supply agreement by the commercial supplier resulting in a Radius breach of the CSA, to pursue any potential claims against commercial supplier on behalf of Teijin to the extent required under the CSA.

The CSA will remain in effect, unless terminated earlier for breach, until the earlier of the expiration or termination of the LDA, the expiration or termination of Radius’s commercial supply agreement with the commercial supplier, or termination by either party in the event of the other party’s bankruptcy.

Appointment of Chief Executive Officer

On July 28, 2022 Fusion Antibodies plc (AIM: FAB), specialists in pre-clinical antibody discovery, engineering and supply for both therapeutic drug and diagnostic applications, reported the appointment of Dr Adrian Kinkaid as Chief Executive Officer ("CEO"), effective from Monday 15 August 2022 (Press release, Fusion Antibodies, JUL 28, 2022, View Source [SID1234617267]). Adrian’s appointment follows an extensive formal search process further to the Company’s announcement on 14 March 2022.

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Adrian Kinkaid is an experienced life sciences executive with 25 years’ experience in life science and biotherapeutics industries. He joins Fusion from Vortex Liquid Biopsy Solutions Ltd and Vortex Biosciences Inc. (together "Vortex"), a biotech group focused on world class technology for the isolation of high quality circulating tumour cells. As CEO of Vortex, Adrian led the company’s development, including management of its business units.

Prior to joining Vortex, Adrian worked as CEO at several antibody-based diagnostics companies including BioFab Ltd, and Lumabs BV. He was formerly the Chief Commercial Officer for Promexus Ltd, a protein biotherapeutics company where he developed the corporate strategy for Therapeutic Affimers, culminating in a multi-target deal with a potential of over $1bn. Adrian was previously Chief Business Officer of the Aptamer Group, and Strategic Market Development Leader for Abcam plc, the leading provider of research antibodies.

Adrian has a PhD in Biochemistry and undertook postdoctoral research with the Institute of Cancer Research, London. As Chairman and founding member of the European Laboratory Research and Innovation Group, Adrian established their flagship Drug Discovery event, which is now the leading conference of its kind in Europe.

Simon Douglas, Chairman of Fusion Antibodies, commented: "I would like to welcome Adrian who joins Fusion at an exciting time as we focus on growing our antibody services and completing the development of and commercial roll out next year of OptiMAL, our Mammalian Antibody library."

Adrian Kinkaid said: "I am delighted to be joining Fusion Antibodies at this exciting time of growth and look forward to leading the Company to further commercial success. Fusion Antibodies has a world class technology platform built over the last decade that has the potential to generate significant value and play a global role in the provision of high quality services to enhance the discovery and development of novel, effective antibody therapeutics."

Takeda Quarterly Financial Report for the Quarter Ended June 30, 2022

On July 28, 2022 Takeda reported its second quarter 2022 results (Presentation, Takeda, JUL 28, 2022, View Source [SID1234617152]).

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10-Q – Quarterly report [Sections 13 or 15(d)]

Seagen has filed a 10-Q – Quarterly report [Sections 13 or 15(d)] with the U.S. Securities and Exchange Commission .

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