CLINUVEL PHARMACEUTICALS LTD released its Appendix 4C – Quarterly Cashflow Report and Activity Report for the period 01 July to 30 September 2022.

On November 1, 2022 CLINUVEL recorded its highest quarterly results from customer receipts since the commencement of commercial operations in Europe in June 2016 and United States in April 2020 (Press release, Clinuvel, NOV 1, 2022, View Source;mc_eid=a3338e0afe [SID1234622637]). New patient uptake of CLINUVEL’s drug SCENESSE (afamelanotide 16mg) coincided with peak treatment demand from both continents. CLINUVEL’s receipts from customers for the July to September quarter were $25.152 million, with net operating expenditures of $8.270 million and net operating cashflow totalling $17.338 million.

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The quarter-on-quarter increase of overall net operating expenditures (47%) reflects the impact of the timing of certain payments as well as a controlled increased in overall expenditures as CLINUVEL expands its R&D activities. On an annual basis, operating expenditures demonstrates a 31.9% increase for the 12 months to 30 September 2022, indicating an ongoing commitment to re-invest in the business.

FULL YEAR DIVIDEND
Total cash reserves were impacted by CLINUVEL paying, on 21 September 2022, a
full year unfranked dividend distribution of $0.04 per share, translating to a $1,976,000 payment to registered holders. This was a 60% increase to the dividend distribution made in September 2021. The strong performance of the Company for the 2021/22 financial year allowed the Board to declare the increase in dividend, most of all recognising the loyalty and patience of long-term shareholders.

"The positive net cash inflow results reflects the demand over the spring and summer months in the northern hemisphere, the efficiency of the Company’s commercial infrastructure, coupled with a focus on containing cost increases," CLINUVEL’s Chief Financial Officer, Darren Keamy said.

"The growth in the cash position enables management to dedicate itself to pursuing further strategic initiatives, while research and development are ongoing to expand the Company’s pipeline. Global economic conditions are dire and an energy crisis is looming in many parts of the world, yet we are on course to realise CLINUVEL’s growth plans, allowing us to come out stronger when the global economies recover."

POSITION TO SELF-FINANCE GROWTH
CLINUVEL has communicated a strategic commitment to spend $175m on the growth of the business over the five years to 30 June 2025. Expenses are steadily increasing but well within the window projected for its Pharmaceutical and Healthcare Solutions Divisions to expand clinical use of SCENESSE and to add new products. The Company’s investments remain on track with its forecast with just over $55 million spent in FY2021/22, and therefore, around $120 million to be expended over the next three years. This excludes capital expenditures.

KEY ACTIVITIES
Key activities in the September quarter 2022 are summarised below.
Commercial Operations
During the past quarter, treatment was extended to more patients and the close relationships with healthcare professionals, insurers, and government agencies continued to facilitate access to treatment for erythropoietic protoporphyria (EPP) patients.

Progress of Clinical Programs
CLINUVEL is focused on an expanded range of targeted clinical development programs evaluating the safety and efficacy of melanocortins – including afamelanotide – for patients with genetic, metabolic, life-threatening and acute disorders. A summary of the clinical programs is provided below:

Healthcare Solutions
CLINUVEL differentiates itself from most pharmaceutical companies by translating its expertise and technology (the class of melanocortins) to non-prescription products for wider use and for specialised populations in need of strong and long term skin care. These populations are characterised as being at Highest Risk of photodamage and skin cancers.

CLINUVEL continues to work towards the launch of a range of dermatocosmetic products aimed at specialised populations at highest risk from exposure to ultraviolet (UV) and high energy visible (HEV) light. The first product CYACÊLLE provides polychromatic protection against light in the invisible and visible spectrum. Research & development of future product lines is underway. These products will assist in DNA repair of affected skin, while aiming to stabilise melanogenesis.

Ahead of formal product launch, staggered digital marketing campaigns are underway to establish specialized audiences at highest risk of solar damage and prone to skin cancers and melanoma. New digital platforms, including LightSkinScience.com, and dedicated social media channels have been launched, with a team of CLINUVEL Ambassadors (CUVAs) engaged to educate and build connectivity with the targeted audiences.

Other Activities and Announcements

The Company’s Annual Report for the past financial year (ended 30 June 2022) was
announced on 30 August 2022 and, following a briefing to shareholders first in Basel and later in Monaco, the Company released its fifth Strategic Update on 19 September. The Company’s announcements in the September quarter 2022 are available on the CLINUVEL website, with other updates available on the CLINUVEL News website.

Although the Company is no longer obligated under ASX Listing Rules to publish quarterly cash flow results, it elects to continue to do so to keep its global investors updated regularly. A copy of the Appendix 4C – Quarterly Cash Flow Report for the final quarter of FY2022 is attached.
Pursuant to Listing Rule 4.7C and as disclosed in Item 6.1 to the attached
Appendix 4C, $2,648,000 were recorded in respect to Non-Executive Directors’
fees, Managing Director’s fees and payments towards non-monetary benefits
(inclusive of short-term incentive and long-term retention benefit entitlement
to Managing Director).
1 SCENESSE (afamelanotide 16mg) is approved in the European Union and Australia as an orphan medicinal product for the prevention of phototoxicity in adult patients with erythropoietic protoporphyria (EPP). SCENESSE is approved in the USA to increase "pain-free" light exposure in adult EPP patients with a history of phototoxicity. Information on the product can be found on CLINUVEL’s website at www.clinuvel.com.

OncoBone Ventures presented exciting data of its OBP-001 asset in ENA 2022 Symposium

On October 31, 2022 OncoBone Ventures reported the company attended 34th EORTC-NCI-AACR (Free EORTC-NCI-AACR Whitepaper) (ENA) Symposium on Molecular Targets and Cancer Therapeutics in Barcelona, Spain on October 26 – 28 (Press release, OncoBone Ventures, OCT 31, 2022, View Source [SID1234636480]). In the Symposium Tiina Kähkönen, CSO of OncoBone Ventures presented a poster titled "Neutralizing Antibody for S100A8/A9 Soil Sensing Signal to Prevent Metastatic Disease" (you can watch the presentation from the following link: ENA presentation).

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The poster was prepared in collaboration with Okayama University. It shows a summary of the preclinical work demonstrating a role for S100A8/A9 and its receptors in metastasis of melanoma, breast and lung cancer, and development of OBP-001, a neutralizing monoclonal antibody targeting S100A8/A9 that prevents formation of lung metastases in melanoma and breast cancer animal models.

Tiina Kähkönen, CSO of OncoBone Ventures says: "Based on current scientific evidence S100A8/A9 is a potential osteoimmuno-oncology (OIO) target for patients with bone metastases. We will continue by evaluating efficacy of OBP-001 in breast cancer bone metastasis models and are excited to share the progress in future scientific events."

DEFENCE TO APPLY ITS PROPRIATRY ACCUMTM TECHNOLOGY IN THE DESIGN OF MESSENGER RNA ANTI-CANCER VACCINES

On October 31, 2022 Defence Therapeutics Inc. ("Defence" or the "Company"), a Canadian biopharmaceutical company specialized in the development of immuneoncology vaccines and drug delivery technologies, reported that it is initiating a new research and development program designed to exploit the AccumTM technology in engineering messenger (m)RNA vaccines targeting cancer (Press release, Defence Therapeutics, OCT 31, 2022, View Source [SID1234626254]). AccumTM is designed for intracellular accumulation with capabilities to deliver an increased drug delivery to the targeted cells.

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According to Precedence Research, the mRNA therapeutics market size is projected to surpass around USD 128.14 billion by 2030 and growing at a registered CAGR of 13.03% from 2022 to 2030.

The use of the mRNA technology in the formulation of new vaccines has been at the center of focus for many pharmaceutical companies following the successful halting of the SARS-CoV2 pandemic by Pfizer/BioNTech and Moderna’s mRNA vaccines. This new therapeutic modality is currently facing many challenges that may impede its potency. Some of these obstacles include: i) structural complexity of some very large mRNA molecules, ii) the intrinsic instability of mRNA molecules, and more importantly, iii) mRNA sensitivity to degradation by nucleases. Although some of these challenges have been partially solved by means of chemical modification strategies, efficient intracellular delivery of mRNA still represents a major hurdle, which highlights the need of future perspectives/strategies to potentiate this promising new type of medicine.

"The use of mRNA vaccines to combat the SARS-CoV2 pandemic has definitely sparked a major line of interest in the use of this technology for other diseases such as cancer. The success of these mRNA anti-cancer vaccines relies primarily on their ability to escape endosomes to reach the cytoplasm of the cell where the final protein product is generated", says Mr. Plouffe, the CEO of Defence Therapeutics.

With its impressive pre-clinical success on protein-and antibody-based drugs/vaccines, Defence Therapeutics now intends to incorporate its versatile AccumTM technology in the design of anti-cancer vaccines. Defence and its scientific team see that the application of AccumTM makes perfect sense as this platform is specially designed to overcome one "global and limiting step" for any molecular biopharmaceutical: endosomal escape.

"By linking AccumTM to an mRNA molecule, we can ensure that the vaccine is not only delivered to the right cellular compartment, but also accumulates in large amounts to prime an immune response that is at least 50-100-fold higher than standard naked RNA molecules", adds Mr. Plouffe.

The Defence team recently initiated an Accum-mRNA anti-cancer vaccine program targeting solid lymphoma. When completed, the company intends to share its successful story with all major players in the field as it believes that the technology should be exploited in every mRNA vaccine currently in development by the pharmaceutical industry.

Q2 2022 Financial Results (April 2022 to September 2022)

On October 31, 2022 JSR reported its second quarter 2022 Financial Results (April 2022 to September 2022 (Presentation, JSR, OCT 31, 2022, View Source [SID1234624760]).

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FY2022 Q2 Financial Results Presentation

On October 31, 2022 Daiichi Sankyo reported its second quarter financial results (Presentation, Daiichi Sankyo, OCT 31, 2022, View Source [SID1234624534]).

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