Evotec SE: translational BRIDGE partnership beLAB2122 selects oncology project from Goethe University Frankfurt

On July 4, 2022 Evotec SE (Frankfurt Stock Exchange: EVT, MDAX/TecDAX, ISIN: DE0005664809; NASDAQ: EVO) reported that a project has been selected for further development within beLAB2122, a translational BRIDGE collaboration between Evotec and Bristol Myers Squibb (Press release, Evotec, JUL 4, 2022, View Source [SID1234616456]). beLAB2122 aims to bring together leading academic institutions from the Rhine-Main-Neckar region of Germany to efficiently advance first-in-class therapeutic options across all therapeutic areas and formats into investable drug discovery and early development projects.

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The project originates from the lab group of Prof. Dr Ivan Đikić, Molecular biologist and Director of the Institute for Biochemistry II at the Goethe University Frankfurt and was initiated by Innovectis, a technology transfer company of the Goethe University. The project aims at using a bifunctional degrader to selectively target an enzyme with high relevance for the splicing of RNA as a novel pathway in cancer. beLAB2122 will leverage Evotec’s integrated discovery and development platform to validate the approach further and develop a potential first-in-class programme as a treatment for certain cancer types.

beLAB2122 was founded in April 2021 as a translational collaboration between Evotec and Bristol Myers Squibb. The project from the University of Frankfurt marks the second project to be developed within this academic BRIDGE collaboration. The goal of beLAB2122 is to develop academic projects to value inflection points that allow the formation of new jointly owned spin-off companies.

Dr Thomas Hanke, EVP & Head of Academic Partnerships at Evotec, commented: "We are very excited about this project with the Goethe University Frankfurt within the beLAB2122 collaboration. The project addresses a highly promising therapeutic mechanism and holds the potential for a novel oncology treatment. With BRIDGE collaborations such as beLAB2122, Evotec aims at accelerating academic innovations into drug discovery to allow new company formations. We are keen to see the first results and look forward to progressing this and many more interesting academic projects."

Prof. Dr Ivan Đikić, Molecular biologist and Director of the Institute for Biochemistry II at the Goethe University Frankfurt, added: "This programme offers an excellent opportunity for academic researchers to collaborate with pharma partners in the early discovery stage. The major benefit of working together is to provide faster and better validation of promising therapeutic targets and enable rapid translation, e.g. by creating jointly owned spin-off companies. This also adds an important facet to scientific training and is therefore of enormous value to Goethe University."

Sareum notes GSK’s completed acquisition of Sierra

On June 4, 2022 Sareum Holdings plc (AIM: SAR), the specialist drug development company, reported that GSK has completed its acquisition of Sierra Oncology, Inc ("Sierra"), the licence holder for SRA737 (a novel Chk1 inhibitor), for US$1.9 billion in cash (Press release, Sareum, JUL 4, 2022, View Source [SID1234616454]). The acquisition was approved by Sierra’s shareholders on 29 June 2022.

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GSK has noted that the key driver of the acquisition was momelotinib, a drug Sierra is developing for the treatment of myelofibrosis. Sierra reported positive topline results from a Phase III study investigating momelotinib in this indication in January 2022 and submitted a New Drug Application ("NDA") to the US Food and Drug Administration ("FDA") in June 2022 for marketing approval.

Following the acquisition, GSK also now owns the licence rights to SRA737, a clinical-stage oral, selective Checkpoint kinase 1 inhibitor that targets cancer cell replication and DNA damage repair mechanisms. SRA737 was discovered and initially developed by scientists at The Institute of Cancer Research in collaboration with Sareum, and with funding from Sareum and Cancer Research UK. SRA737 was licensed to Sierra in September 2016 and has progressed through multiple preclinical and early-stage clinical trials demonstrating potential for further investigation in combination with other agents in haematologic and solid tumour indications.

Under an amended US$299m licensing deal on SRA737 between Sierra and CRT Pioneer Fund LP (announced 12 November 2020), Sareum is eligible to receive a 27.5% share of any future milestone payments as well as royalties on any future sales. The dosing of the first patient with SRA737 in any new clinical trial would result in a US$2.0m payment from Sierra (now GSK), with 27.5% of this due to Sareum.

Transactions in connection with share buy-back program

On July 4, 2022 Genmab reported the initiation of a share buy-back program to mitigate dilution from warrant exercises and to honor our commitments under our Restricted Stock Units program (Press release, Genmab, JUL 4, 2022, View Source [SID1234616453]).

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The share buy-back program is expected to be completed no later than August 31, 2022 and comprises up to 370,000 shares.

The following transactions were executed under the program from June 27, 2022 to July 1, 2022:

Details of each transaction are included as an appendix to this announcement.

Following these transactions, Genmab holds 362,885 shares as treasury shares, corresponding to 0.55% of the total share capital and voting rights.

The share buy-back program is undertaken in accordance with Regulation (EU) No. 596/2014 (‘MAR’) and the Commission Delegated Regulation (EU) 2016/1052, also referred to as the "Safe Harbour Regulation." Further details on the terms of the share buy-back program can be found in our company announcement no. 22 dated June 17, 2022.

PAT-DX1 Engineering Run Successfully Completed

On July 4, 2022 Patrys has reported a positive update on the second engineering run for its lead asset PAT-DX1, a critical step for ensuring we can manufacture at commercial scale (Press release, Patrys, JUL 4, 2022, View Source [SID1234616450]).

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This follows an earlier set-back when the first engineering run for PAT-DX1 was unsuccessful due to low recoveries of drug product during the purification phase.

Patrys CEO and MD, Dr James Campbell, was delighted to share the news today:

"This is an outstanding result, and a tribute to the close working relationship between Patrys and our CDMO. The commercial‑scale manufacture of antibodies is a complex, multi‑dimensional process. The efforts made to understand and remediate the issues with the first engineering run have been both extensive and exhaustive. We are delighted that this has delivered such a successful outcome."

Shanghai Junshi Biosciences Co., Ltd. and Risen Pharma Tech Co., Ltd. Announces FDA Approval of Investigational New Drug Application for JS105

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