NOXXON to Attend the German Fall Conference on September 6 & 7, 2021

On August 25, 2021 NOXXON Pharma N.V. (Euronext Growth Paris: ALNOX), a biotechnology company focused on improving cancer treatments by targeting the tumor microenvironment (TME), reported that it will participate in the German Fall conference taking place from September 6 to September 7, 2021 (Press release, NOXXON, AUG 25, 2021, View Source [SID1234586888]). The capital market conference for small and mid-cap companies organized by Equity Forum will take place in the form of virtual one-on-one meetings.

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The conference aims at bringing together public company representatives across sectors with investors, analysts, financial journalists, intermediaries and financial industry experts. Around 100 companies will participate in this year’s summit to present their equity story. NOXXON’s CEO, Aram Mangasarian, will be available for meetings on both conference days. To schedule a meeting please contact the conference organizer or send an email to [email protected].

Bavarian Nordic Announces First Half 2021 Results

On August 25, 2021 Bavarian Nordic A/S (OMX: BAVA) reported its interim financial results and business progress for the first half of 2021 and releases its financial calendar for 2022 (Press release, Bavarian Nordic, AUG 25, 2021, View Source [SID1234586887]).

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Paul Chaplin, President & Chief Executive Officer of Bavarian Nordic said: "We are very pleased to confirm the successful execution of our commercial strategy with nearly 30 Rabipur/RabAvert and Encepur markets now transferred to Bavarian Nordic. Our objective during this transition was to stop the historical market share losses before the acquisition of these products, start gaining more ground and increase the awareness of Bavarian Nordic among health care professionals and we are pleased that we today can tick all these boxes, despite that the markets are still impacted by COVID-19. Both the rabies and TBE markets are still suffering from a low level of international travel and limited availability of physicians for non-COVID vaccinations in certain markets and due to this alone, we are firming up our financial guidance for 2021 to reflect the lower end of the previously guided intervals.

So far this year, we also received new orders for our Ebola and smallpox vaccines and saw very important advancements in our pipeline assets with our promising COVID-19 vaccine candidate, ABNCoV2 entering Phase 2 after reporting highly promising clinical results. The recent agreement with the Danish Ministry of Health to provide aid for developing ABNCoV2 is a strong recognition of the technology and Bavarian Nordic to develop a highly promising general booster against COVID-19. With this funding, together with our existing commitment to fund the program to the end of Phase 2, we have sufficient funds to execute the existing plans to develop ABNCoV2 through to licensure. We look forward to reporting the Phase 2 results for ABNCoV2, as well as additional pivotal results from the RSV human challenge trial later this year."

Financial highlights

Total revenue in first half year was DKK 905 million comprised of DKK 877 million from combined product sales and DKK 28 million from contract work.
Revenue in second quarter totaled DKK 370 million comprised of DKK 146 million from sale of Encepur, DKK 127 million from sale of Rabipur/RabAvert, DKK 89 million from sale of Mvabea to Janssen and DKK 8 million from contract work.
EBITDA in first half year was a loss of DKK 8 million.
Strong cash position of DKK 2,208 million at the end of the first half, excluding unutilized credit facilities of DKK 243 million and after deduction of repo pledged securities.
Full-year guidance maintained at the lower end of the previously guided ranges, due to the continued COVID-19 impact on the TBE and rabies markets. Thus, revenue of approximately DKK 1,900 million, EBITDA of approximately DKK 100 million and securities, cash and cash equivalents at year-end of approximately DKK 1,400 million are expected.

Events in the second quarter

In April, new preclinical results for the COVID-19 vaccine candidate, ABNCoV2 were announced, confirming its potential to offer broad protection against variants of the SARS-CoV2 virus.
In April, Bavarian Nordic received a new Ebola supply order from Janssen, valued at approximately USD 28 million. Manufacturing and delivery will occur during 2021. The Johnson & Johnson Ebola vaccine regimen, which includes Mvabea from Bavarian Nordic also received Prequalification from the World Health Organization, which along with the July 2020 approval from the European Commission, will help accelerate its registration in countries where Ebola is a persistent public health threat.
In May, the US government exercised the final USD 12 million option remaining under the USD 202 million order for JYNNEOS awarded in April 2020.
In May, Bavarian Nordic entered an agreement with Dynavax on marketing and distribution of their HEPLISAV B hepatitis B vaccine in Germany.
Events after the reporting date

In August, Bavarian Nordic entered a funding agreement with the Danish Ministry of Health, under which the Company will be eligible to receive up to DKK 800 million to further advance the development of ABNCoV2 as a booster vaccine for COVID-19.
In August, Bavarian Nordic initiated a Phase 2 clinical trial of ABNCoV2 to investigate the vaccine’s potential as a universal booster vaccine for individuals with existing immunity from prior COVID-19 disease or vaccination.
In August, initial results from the first-in-human trial of ABNCoV2 were reported, showing that the vaccine candidate was well tolerated and induced a strong antibody response, superior to current approved vaccines. Importantly, a strong neutralization response was demonstrated against SARS-CoV2 variants, including the Delta variant.
The Company has today published its financial calendar for 2022, which is available on page 8 in this report.
Conference call and webcast
The management of Bavarian Nordic will host a conference call today at 2 pm CET (8 am EST) to present the interim results followed by a Q&A session. A listen-only version of the call can be accessed via View Source To join the Q&A session, use one of the following dial-in numbers: Denmark: +45 32 72 80 42, UK: +44 (0) 844 571 8892, USA: +1 631-510-7495. Participant code is 8569159.

Neuren Pharmaceuticals Limited
Appendix 4D Half-Year Financial Report
30 June 2020

On August 25, 2021 Neuren Pharmaceuticals Limited ("Neuren" or the "Company") reported this financial report, including the interim consolidated financial statements, for the six months ended 30 June 2020, with the six months ended 30 June 2019 as the comparative period.

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2. Results for announcement to the market

The Group’s net loss after tax for the half-year ended 30 June 2020 was $4.8 million, compared with $7.9 million for the half-year ended 30 June 2019, predominately due to a decrease of $2.7 million in research and development costs. This was due to lower expenditure for manufacturing and non-clinical activities relating to the Rett Syndrome Phase 3 trial, partially offset by an increase in expenditure in 2020 for the NNZ-2591 non-clinical studies and Phase 1 trial, including manufacture of the required drug.

A more detailed discussion of the activities undertaken in the period is set out in the Directors’ Report contained in the attached Interim Report.

3. Net Tangible Assets per Security

4. Entities over which control has been gained or lost during the period: None.

5. Details of dividends Not applicable.

6. Details of dividend reinvestment plans Not applicable.

7. Details of associates and joint venture entities None.

8. Accounting standards The interim financial statements have been prepared in accordance with generally accepted accounting practice in New Zealand and NZ IAS 34 Interim Financial Reporting.

9. Auditors review
The interim financial statements have been subject to independent review by the Company’s auditors. The unqualified review report is included in the attached Interim Report

United Therapeutics Partners with Former NFL Player Devon Still and His Daughter Leah to Launch "Braving NeuroBLASToma" in Honor of Childhood Cancer Awareness Month

On August 25, 2021 United Therapeutics Corporation (Nasdaq: UTHR) reported it is joining forces with former NFL player Devon Still and his daughter Leah, a survivor of high-risk neuroblastoma, to launch the educational initiative "Braving NeuroBLASToma" shining a light on the rare cancer affecting immature nerve cells called neuroblasts.iv Neuroblastoma often develops in infants and children under the age of five, but the average age of diagnosis is between one and two years old (Press release, United Therapeutics, AUG 25, 2021, View Source [SID1234586885]).

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Devon and Leah Still, spokespeople for Braving NeuroBLASToma

Each year, about 800 children are diagnosed with neuroblastoma, accounting for seven to ten percent of all childhood cancers in the United States. v, vi At the time of diagnosis, nearly 70 percent of children will have advanced or metastatic neuroblastoma, with only half of these patients achieving remission.vii,viii Neuroblastoma can start to form in several places including near the abdomen, spine, chest, or adrenal glands.ix

"When I first learned that Leah had high-risk neuroblastoma, the sense of fear and helplessness was so overwhelming that I struggled to know where to begin," said Devon Still. "Over the years, so many in the childhood cancer community have shown us how much they care each and every step of the way, from making the tough decisions to ensuring Leah’s comfort while undergoing treatment. Partnering with United Therapeutics enables us to share our personal experiences with braving neuroblastoma and lend others the support we so generously received throughout the years."

Braving NeuroBLASToma features:

A family-friendly toolkit with a resource-rich website, including a comprehensive library of information and resources such as questions for the doctor, navigating clinical trials, understanding treatment, and caregiver advice.
A series of four beautifully illustrated books, including the latest release of Zara Takes Off – inspiring hope and encouragement as families transition to life after treatment. The new release includes a personal foreword penned by Leah, sharing details of her personal journey.
Each book highlights different stages of the high-risk neuroblastoma journey, beginning with The Big Adventures of Little Skivolo that helps families understand diagnosis and treatment, The Next Big Adventure of Little Skivolo that focuses specifically on the antibody therapy phase of treatment, Little Skivolo’s Big Book of Fun, an activity book to help entertain kids and families during hospital stays and culminates with Zara Takes Off. 
"For many years, United Therapeutics has been working with leading researchers in pediatric neuroblastoma, including the Children’s Oncology Group supported by the National Cancer Institute, to bring hope to thousands of families fighting this deadly childhood cancer," said Karren Jackson, Oncology Program Head at United Therapeutics. "We are tremendously proud to partner with Devon Still and his daughter Leah to highlight what courage, resilience and support from loved ones can do for children and their families impacted by neuroblastoma."

As treatment comes to an end, families can start to transition out of treatment mode and into more familiar routines while the healthcare team continues to monitor the child’s recovery. But the neuroblastoma journey doesn’t stop there, patients will continue to see their oncology team on a routine basis to monitor for long-term side effects and to ensure the cancer has not returned. This leg of the journey requires continued vigilance, support, and encouragement.

"The treatment of a child with high-risk neuroblastoma challenges both patients and caregivers to their core, with each family enduring unique and evolving medical needs," said Rochelle Bagatell, MD, Pediatric Oncologist, Children’s Hospital of Philadelphia, and Neuroblastoma Committee Chair for the Children’s Oncology Group. "As a care provider, I encourage families to leverage the resources available to them, so together we can ensure that each child receives the best care and support possible."

For more information visit BravingNeuroBLASToma.com, a comprehensive resource for every step in the patient journey.

About Neuroblastoma:
Neuroblastoma is the most common cancer in infants less than a year old, but is considered a rare cancer.i Each year, about 800 children are diagnosed with neuroblastoma, accounting for seven to ten percent of all childhood cancers in the United States.v,vi This solid-tumor cancer starts in immature nerve cells called neuroblasts and often develops in infants and children under the age of five, but the average age of diagnosis is between one and two years old.iv Neuroblastoma can form anywhere along the sympathetic nerve chain and is commonly seen in in the abdomen, spine, chest or adrenal glands.ix At the time of diagnosis, nearly 70 percent of children will have advanced or metastatic neuroblastoma.vii Despite advancements in the research and approval of treatments for neuroblastoma, there remains a high unmet need for high-risk neuroblastoma patients. For children with pediatric high-risk neuroblastoma, even when treated and remission is achieved, about 50-60% will relapse (disease returns) and about 10% of children with pediatric high-risk neuroblastoma will not respond to upfront chemotherapy—this is called refractory neuroblastoma.x There is currently no cure for relapsed high-risk neuroblastoma.xi

PROMIS NEUROSCIENCES CLOSES UPSIZED US$20,125,000 PUBLIC OFFERING 

On August 25, 2021 ProMIS Neurosciences Inc. (TSX: PMN) (the "Company" or "ProMIS"), a biotechnology company focused on the discovery and development of antibody therapeutics targeting toxic oligomers implicated in the development of neurodegenerative diseases, reported that it has closed its previously announced upsized public offering (the "Offering") for gross proceeds of US$20,125,000, including the exercise in full of the 15% Agent’s option (Press release, ProMIS Neurosciences, AUG 25, 2021, View Source [SID1234586883]).

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A total of 125,781,250 units of the Company (the "Units") were issued at US$0.16 per Unit pursuant to the Offering. Each Unit consisted of one common share of the Company (a "Common Share") and one-quarter of one Common Share purchase warrant (each whole purchase warrant, a "Warrant"). Each Warrant entitles the holder thereof to purchase one Common Share (each, a "Warrant Share") at a price of US$0.21 per Warrant Share at any time up to August 25, 2026, subject to an acceleration provision.

Leede Jones Gable Inc. (the "Agent") acted as the agent and sole bookrunner pursuant to an agency agreement with the Company dated August 19, 2021 (the "Agency Agreement"), and Ceros Financial Services, Inc. acted as the exclusive sub-agent for the sale of Units in certain jurisdictions.

In consideration for the services performed by the Agent pursuant to the Agency Agreement, the Company paid the Agent (or as the Agent otherwise directed) a cash commission equal to 7% of the gross proceeds from the Offering and issued to the Agent (or as the Agent otherwise directed) that number of compensation warrants (the "Compensation Warrants") equal to 7% of the Units sold under the Offering. Each Compensation Warrant entitles the holder thereof to purchase one Common Share (each, a "Compensation Warrant Share") at a price of $0.16 per Compensation Warrant Share at any time up to August 25, 2026.

The Offering was made pursuant to the Company’s prospectus supplement dated August 19, 2021 (the "Supplement") to the Company’s short form base shelf prospectus dated June 30, 2021 (the "Base Prospectus"). Additionally, the Offering was conducted by way of private placement in other jurisdictions where the Offering could lawfully be made. Copies of the Base Prospectus, Supplement and Agency Agreement are available under the Company’s profile on SEDAR at www.sedar.com.

The Company intends to use the net proceeds from the Offering to advance its lead Alzheimer’s therapy PMN310 to the filing of an Investigational New Drug (IND) application to enable a first clinical trial; to expand the Company’s portfolio of antibodies and patents; and for general corporate purposes, including, to establish a discovery laboratory in the Boston area, to accelerate and broaden the scope of the Company’s discovery efforts and to add additional scientific, administrative and support staff, all as further set out in the Supplement.

The investors include Mike Gordon of Fenway Sports Group, the Kraft Group, Henry McCance, cofounder of the Cure Alzheimer’s Fund, and Jeremy Sclar of WS Development Group, all of whom invested in the March 2021 financing, as well as new investors David Adelman of Darco Capital, Michael Rubin, Chairman and CEO of Fanatics, and Aspire Capital Fund, an institutional investor based in Chicago.

The securities being referred to in this news release have not been, nor will they be, registered under the United States Securities Act of 1933, as amended, and may not be offered or sold in the U.S. or to, or for the account or benefit of, U.S. persons absent registration or an applicable exemption from the registration requirements. This news release does not constitute an offer to sell or the solicitation of an offer to buy nor shall there be any sale of the securities in any jurisdiction in which such offer, solicitation or sale would be unlawful.