Evotec expands clinical and commercial drug substance manufacturing with acquisition of Central Glass Germany

On August 25, 2022 Evotec SE (Frankfurt Stock Exchange: EVT, MDAX/TecDAX, ISIN: DE0005664809; NASDAQ: EVO) reported that the Company expands its clinical and commercial manufacturing platform for small molecule therapeutics by acquiring Central Glass Germany GmbH from the Japanese chemical manufacturing company Central Glass Co. Ltd (Press release, Evotec, AUG 25, 2022, View Source [SID1234618650]).

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Going forward, Central Glass Germany GmbH will operate as Evotec Drug Substance (Germany) GmbH ("Evotec DS"). The Company is located on a pharmaceutical manufacturing campus in Halle/Westphalia, Germany and is operating with a team of ~60 chemical manufacturing experts. The facility is EU cGMP certified and provides highly flexible drug substance manufacturing space with over 5,000 square meters of floor space.

The acquisition of the Central Glass site in Germany enhances and accelerates Evotec’s strategy of pursuing integrated discovery and development of new medicines that matter. The significant reactor capacity and long-standing chemical expertise brought in by Evotec DS provide a high quality, European-based solution to Evotec’s partners for the development and commercialisation of drug substance. Once integrated into Evotec’s existing drug substance development and manufacturing platform, the new site will offer the Company’s partners highly flexible product lifecycle management strategies, particularly in the field of precision medicines and in rare diseases.

Dr Werner Lanthaler, Chief Executive Officer of Evotec, commented: "Our understanding of diseases continuously grows in depth – and with it the number of rare diseases that we can meaningfully distinguish and target with precision medicine. Evotec DS reinforces our commitment to rare diseases by integrating the manufacturing of such drugs into the drug discovery and development continuum. We very warmly welcome the team into the Evotec family and are excited to leverage their skills and expertise for our partners."

The contract was signed on 24 August at a purchase price of € 1. The transaction is subject to customary closing conditions and is anticipated to close on 1 November 2022. Evotec intends to invest meaningfully in the coming years to establish the facility as a leading European centre of excellence for rare disease drug substance manufacturing. Earnings accretion is expected to be achieved by 2023/24.

Interim report for the period January 1, 2022 – June 30, 2022

On August 25, 2022 Vivesto AB reported that Interim report for the period January 1, 2022 – June 30, 2022 (Press release, Vivesto, AUG 25, 2022, View Source [SID1234618649]).

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SIGNIFICANT EVENTS DURING THE SECOND QUARTER
In April Daniel Tesfa was appointed Chief Medical Officer.
In April Vivesto signed an agreement with leading US CRO Visikol Inc. to evaluate anti-cancer drug formulations using, among other things, its proprietary drug delivery platforms.
In May the Annual General Meeting resolved on re-election of Hege Hellström and Peter Zonabend as well as new election of Pål Ryfors and Roger Tell as members of the Board of Directors. Anders Härfstrand, Andrea Buscaglia and Birgit Stattin Norinder had declined re-election. Peter Zonabend was elected as Chairman of the Board.
In June Vivesto announced that the Board of Directors of the company had agreed with the company’s CEO, Francois Martelet, to mutually terminate his employment as of 21 July 2022.
In June Robert Maiorana was appointed acting CFO, with effect from July 1, 2022.
SIGNIFICANT EVENTS AFTER THE REPORTING PERIOD
In August, Vivesto’s and Elevar’s partner Inceptua began the commercial launch of Apealea in Germany.
In July Vivesto announced that the company has decided to wind down its activities in Russia following the Russian invasion of Ukraine, ongoing hostilities and international sanctions. The wind down of Vivesto’s activities in Russia means that a write down of SEK 44.6 million is carried out during the third quarter of 2022, equal to the net book value of the capitalized development costs for Paclical after amortization as of June 30, 2022.
In July Christer Nordstedt was appointed acting CEO. Christer Nordstedt will hold the position until the recruitment of a permanent CEO is completed.
SECOND QUARTER: APRIL 1, 2022 – JUNE 30, 2022
Consolidated net sales amounted to TSEK 0 (4,596)
Operating profit/loss was TSEK -36,323 (-56,165)
Net profit/loss after tax amounted to TSEK -38,514 (-57,677)
Earnings per share amounted to SEK -0.07 (-0.12)
THE PERIOD: JANUARY 1, 2022 – JUNE 30, 2022
Consolidated net sales amounted to TSEK 0 (4,633)
Operating profit/loss was TSEK -62,652 (-97,007)
Net profit/loss after tax amounted to TSEK -64,971 (-98,886)
Earnings per share amounted to SEK -0.13 (-0.22)
Short-term investments, cash and cash equivalents amounted to TSEK 188,828 (176,302)
Equity/assets ratio was 95% (77%)
CEO REVIEW
It is an honor to have taken up the role of acting CEO here at Vivesto in mid-July. As a Doctor and scientist I am proud and glad to be leading a company that is focused on developing medicines for hard-to-treat cancers where there remains such a high unmet medical need. My first few weeks in the role have been highly engaging and I’ve really enjoyed getting to know the Vivesto team and doing a deep dive into each of our development programs. As acting CEO I aim to lead Vivesto to the best of my ability until a permanent replacement is appointed. The last quarter has been a time of change for Vivesto with new recruits and appointments among the senior leadership team.
Daniel Tesfa M.D. Ph.D., our new Chief Medical Officer joined the business in early July and he is responsible for leading the clinical development of our oncology programs. Daniel brings extensive experience in clinical development and precision oncology, most recently, from Swedish biopharmaceutical company SOBI (Swedish Orphan Biovitrum AB), where he led clinical development. Daniel has already made a positive impact and is working very closely with our Chief Scientific Officer, Reinhard Koenig, M.D. PH.D. Robert Maiorana was appointed to the role of acting Chief Financial Officer from 1 July. Robert has worked at Vivesto since the second half of 2020 and as Finance Manager since March 2021 and is thus well familiar with the business and the company. The search for a permanent Chief Financial Officer is ongoing.
The financial markets for listed biotech companies have been challenging during last quarter with increasing concerns about the impact of rising inflation and the resulting cost to business. Geopolitical tensions have also added to business uncertainty. In early July, Vivesto announced that, like most other companies, we have decided to wind down operations in Russia as a result of Russia’s invasion of Ukraine. This meant that distribution activities for Paclical (Apealea) in Russia and the Commonwealth of Independent States (CIS) have been paused until further notice. The challenging macroeconomic environment and geopolitical tensions in eastern Europe are beyond Vivesto’s control, but today we are in a resilient position as we are well capitalized following the rights issue earlier this year and we hold no debt.
We remain focused on adding value by developing new cancer medicines and and new treatment options. Preparations for the next clinical study of Cantrixil for metastatic ovarian cancer are ongoing. Docetaxel micellar is being evaluated in a Phase I investigator-initiated trial in metastatic prostate cancer instigated by the Swiss Group for Clinical Cancer Research (SAKK). Recruitment is progressing steadily and we look forward to the completion.
We have been in regular contact with our global strategic partner Elevar over the last quarter. Inceptua, Elevar’s distribution partner in Europe, continues to work on the launch of Apealea. In August, Inceptua announced the launch of Apealea in Germany. This is an important milestone as Germany is the first major global market where Apealea has been commercially launched. In the UK Inceptua is interacting with National Health Service (NHS) to secure reimbursement for Apealea. Until now Inceptua has secured a maximum list price for Apealea allowing private market access to the drug. The launches in Europe are out of our direct control and we continue to give our full support to Elevar and Inceptua to maximize the chances of success when the launch of Apealea proceeds on a country-by-country basis over the next couple of years.
In April we announced that we had signed a research agreement with Visikol Inc., a prominent U.S. contract research services provider, for Visikol to evaluate, among other things, the cellular effects of new and existing anti-cancer drug formulations developed using Vivesto’s XR-17 and XR-18 technologies. This will allow us to select promising developmental drug candidates and further expand our current and future oncology pipeline focused on hard-to-treat and late-stage cancers. I look forward to sharing more information with you in due course when it is appropriate to do so.
Many thanks for your continued support.

Christer Nordstedt, acting CEO of Vivesto

The report is available on the company’s website: View Source

Invitation to presentation of Vivesto’s Q2 report
Vivesto will hold a conference call and an online presentation of the Q2 report on August 25, 2022, at 10.00 am CEST. The call will be hosted by Acting CEO Christer Nordstedt and Acting CFO Robert Maiorana. The presentation will be in English and followed by a question-and-answer session. The conference call will be broadcast live on the web via the link:
View Source

Evogene Regains Compliance with Nasdaq Minimum Closing Bid Price Rule

On August 25, 2022 Evogene Ltd. (Nasdaq: EVGN, TASE: EVGN) (the "Company", "Evogene"), a leading computational biology company targeting to revolutionize life-science product discovery and development across multiple market segments, reported the receipt of a formal notification from The Nasdaq Stock Market LLC ("Nasdaq") that the Company has regained compliance with Listing Rule 5450(a)(1), which requires the Company’s ordinary shares to maintain a minimum bid price of $1.00 per share (Press release, Evogene, AUG 25, 2022, View Source [SID1234618647]).

The Nasdaq staff made this determination of compliance after the closing bid price of the Company’s ordinary shares was at $1.00 per share or greater for the prior 10 consecutive business days. Accordingly, the Company has regained compliance with Nasdaq Listing Rule 5450(a)(1) and Nasdaq considers the prior bid price deficiency matter now closed.

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Iovance Biotherapeutics Initiates Biologics License Application (BLA) Submission for Lifileucel in Advanced Melanoma

On August 25, 2022 Iovance Biotherapeutics, Inc. (NASDAQ: IOVA), a late-stage biotechnology company developing novel T cell-based cancer immunotherapies, reported that it has initiated a rolling Biologics License Application (BLA) submission to the U.S. Food and Drug Administration (FDA) for lifileucel, a tumor infiltrating lymphocyte (TIL) therapy, in patients with advanced (unresectable or metastatic) melanoma who progressed on or after prior anti-PD-1/L1 therapy, and if BRAF mutation positive, also prior BRAF or BRAF/MEK inhibitor therapy (Press release, Iovance Biotherapeutics, AUG 25, 2022, View Source [SID1234618645]). There are no FDA approved therapies in this treatment setting.

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Frederick Vogt, Ph.D., J.D., Interim President and Chief Executive Officer of Iovance, stated, "Initiating our rolling BLA submission for lifileucel is a significant step towards our goal to deliver the first individualized, one-time cell therapy for melanoma patients with significant unmet need. In parallel, we are executing our on-boarding and personnel training at authorized treatment centers, education and awareness initiatives, internal capacity planning, and launch readiness activities to prepare for commercialization. The FDA is supportive of our regulatory approach, and we look forward to continuing this collaboration throughout the submission and review process."

A rolling BLA allows Iovance to submit portions of the BLA to the FDA on an ongoing basis, which enables the FDA to begin review as early as possible while documents are received. Iovance expects to complete the BLA submission in the fourth quarter of 2022. The rolling BLA submission and eligibility for priority review are benefits available under the FDA’s guidance on expedited programs for serious conditions. The FDA previously granted a regenerative medicine advanced therapy (RMAT) designation for lifileucel in advanced melanoma.

"Lifileucel represents hope and a new treatment for thousands of people with advanced melanoma who have very limited options after they progress on available standard of care," said Kyleigh LiPira, CEO, Melanoma Research Foundation. "Cell immunotherapies are revolutionizing cancer treatment, and we are excited about the potential for the first FDA-approved TIL cell therapy for the treatment of melanoma, which helps us take another step towards finding a cure."

The BLA submission for lifileucel is supported by positive clinical data from the C-144-01 clinical trial in patients with advanced melanoma. Iovance plans to present additional results from the C-144-01 trial at a medical meeting later this year.

Aclaris Therapeutics Announces Patent License Agreement with Lilly for Alopecia Areata

On August 25, 2022 Aclaris Therapeutics, Inc. (NASDAQ: ACRS), a clinical-stage biopharmaceutical company focused on developing novel drug candidates for immuno-inflammatory diseases, reported a non-exclusive patent license agreement with Eli Lilly and Company (Lilly) (Press release, Aclaris Therapeutics, AUG 25, 2022, View Source [SID1234618644]).

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Under the license agreement, Aclaris granted Lilly non-exclusive rights under certain patents and patent applications that Aclaris exclusively licenses from The Trustees of Columbia University in the City of New York, for the use of baricitinib, Lilly’s JAK inhibitor, to treat alopecia areata (AA). The agreement includes an upfront payment, regulatory and commercial milestones, and royalties.

"We are pleased to sign this patent license agreement with Lilly," said Jim Loerop, Chief Business Officer of Aclaris. "We believe access to this patent portfolio is necessary for anyone intending to commercialize any JAK inhibitor to treat AA. We have spent considerable resources in licensing and prosecuting our JAK inhibitor patent portfolio and we intend to continue to pursue opportunities provided to us by these patent rights."

Financial terms are not disclosed.