Ascendis Pharma A/S Announces Three Upcoming Investor Presentations

On August 24, 2023 Ascendis Pharma A/S (Nasdaq: ASND) reported that Jan Mikkelsen, President & Chief Executive Officer, and Scott Smith, Executive Vice President & Chief Financial Officer, will participate in three upcoming investor conferences (Press release, Ascendis Pharma, AUG 24, 2023, View Source [SID1234634674]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

Details:

Event Citi’s 18th Annual BioPharma Conference
Location Boston, MA
Date Thursday, September 7, 2023
Time 2:40-3:25 p.m. Eastern Time / 11:40 a.m-12:25 p.m. Pacific Time

Event 2023 Wells Fargo Healthcare Conference
Location Boston, MA
Date Friday, September 8, 2023
Time 8:00-8:35 a.m. Eastern Time / 5:00-5:35 a.m. Pacific Time

Event Morgan Stanley 21st Annual Global Healthcare Conference
Location New York, NY
Date Tuesday, September 12, 2023
Time 12:55-1:25 p.m. Eastern Time / 9:55-10:25 a.m. Pacific Time

A live webcast of the events will be available via the Investors & News section of the Ascendis Pharma website at investors.ascendispharma.com. A webcast replay will also be available on this website shortly after conclusion of the event for 30 days.

Aptose to Present at the H.C. Wainwright 25th Annual Global Investment Conference

On August 24, 2023 Aptose Biosciences Inc. ("Aptose" or the "Company") (NASDAQ: APTO, TSX: APS), a clinical-stage precision oncology company developing highly differentiated oral kinase inhibitors to treat hematologic malignancies, reported that the Aptose management team will participate in the H.C. Wainwright 25th Annual Global Investment Conference being held September 11-13, 2023, in New York City (Press release, Aptose Biosciences, AUG 24, 2023, View Source [SID1234634673]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

Dr. William G. Rice, Chairman, President and CEO of Aptose, will deliver the Company presentation on Monday, September 11, 2023, at 2:00 p.m. ET, and with Mr. Fletcher Payne, CFO of Aptose, will be hosting one-on-one meetings during the conference. To schedule a one-on-one meeting with the Aptose management team, please contact your conference representative.

H.C. Wainwright 25th Annual Global Investment Conference

Date: Monday, September 11, 2023
Presentation Time: 2:00 p.m. ET
Format: Live Presentation, Webcast
Speaker: William G. Rice, PhD, Chairman, President and Chief Executive Officer
Webcast Link: Click here

Recent Clinical Data Highlight with Tuspetinib

Aptose provided a recent update from an ongoing APTIVATE Phase 1/2 clinical trial with the Company’s lead agent, tuspetinib, a once daily oral agent with a unique kinase targeting pattern being developed for the treatment of patients with relapsed/refractory (R/R) AML. As of August 1, 2023, fifteen (15) patients had been dosed with the tuspetinib/venetoclax (TUS/VEN) doublet, ten (10) had reached an efficacy evaluable stage, and five (5) of the ten evaluable patients had achieved early responses (composite Complete Response rate (CRc) includes any CR, CRh, CRi and CRp). Among the ten (10) evaluable patients, nine (9) had failed prior venetoclax treatment (Prior-VEN), representing an emerging population with severe unmet medical need. Four (4) of the nine (9) Prior-VEN failure patients had already achieved responses with TUS/VEN (44% CRc). Three (3) responses emerged among seven (7) of the evaluable patients with wildtype FLT3 (43% CRc), which accounts for approximately 70% of the AML population, yet there are few treatment options and little in development for the wildtype patient population. Additionally, two (2) of three (3) patients with mutated FLT3 (67%) achieved responses. Importantly, The TUS/VEN combination continues to be safe and well tolerated.

AML Subgroup CRc Responses
Evaluable (10) 50% (5 of 10)
Prior-VEN (9) 44% (4 of 9)
FLT3-WT (7) 43% (3 of 7)
FLT3-MUT (3) 67% (2 of 3)

Alpha Tau Medical to Participate in September Investor Conferences

On August 24, 2023 Alpha Tau Medical Ltd. ("Alpha Tau", or the "Company") (NASDAQ: DRTS, DRTSW), the developer of the innovative alpha-radiation cancer therapy Alpha DaRT, reported that management will participate in the following investor conferences (Press release, Alpha Tau Medical, AUG 24, 2023, View Source [SID1234634672]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

Event: Citi’s 2023 Annual BioPharma Conference
Format: 1-on-1 meetings
Date: September 6th, 2023
Location: Boston, MA

Event: Emerging Growth Conference
Format: Company presentation and 1-on-1 meetings
Date: September 7th, 2023
Time 2:20 – 2:50 PM ET
Location: Virtual

Event: Cantor Fitzgerald Global Healthcare Conference
Format: Fireside chat and 1-on-1 meetings
Date: September 27th, 2023
Time: 3:35 – 4:05 PM ET
Location: New York, NY

Please reach out to your Citi and Cantor representatives to schedule, and register here to ensure you are able to attend the Emerging Growth conference and receive any updates that are released.

View Source;tp_key=ab3efc5870&sti=drts

If attendees are not able to join the Emerging Growth Conference live on the day of the conference, an archived webcast will also be made available on EmergingGrowth.com and on the Emerging Growth YouTube Channel, View Source

Alentis Therapeutics Receives FDA Fast Track Designation for ALE.C04 for the Treatment of Claudin-1 Positive HNSCC

On August 24, 2023 Alentis Therapeutics ("Alentis"), a clinical-stage biotechnology company developing treatments for Claudin-1 positive (CLDN1+) tumors and organ fibrosis, reported that the US Food and Drug Administration (FDA) has granted Fast Track development program for ALE.C04 for the treatment of patients with recurrent or metastatic, CLDN1-positive HNSCC (Press release, Alentis Therapeutics, AUG 24, 2023, View Source [SID1234634671]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

Fast Track designation aims to facilitate the development and expedite the review of new medicines that intend to treat serious or life-threatening conditions with unmet medical needs.

"The FDA’s decision to grant Fast Track designation underscores ALE.C04’s potential to address a serious unmet medical need in cancer, specifically HNSCC," said Dr. Roberto Iacone, Chief Executive Officer of Alentis. "We continue to advance our pipeline of antibodies against Claudin-1, an extraordinary target with therapeutic potential across indications in oncology and organ fibrosis."

Dr. Luigi Manenti, Chief Medical Officer of Alentis added, "We are excited with this opportunity to expedite the development of ALE.C04 in patients with recurrent or metastatic, CLDN1-positive HNSCC. The ongoing Phase 1/2 clinical trial in HNSCC will give us important information on ALE.C04’s safety and pharmacodynamic profile as well as its anti-tumor efficacy as monotherapy and in combination with pembrolizumab."

About ALE.C04

ALE.C04 is a first-in-class monoclonal antibody developed to specifically target exposed CLDN1 on cancer cells. This investigational antibody is designed to treat cancer in two ways: remodeling of the extracellular matrix, leading to improved NK and T-cell trafficking and direct tumor cell killing through the effector function. This unique mechanism of action provides ALE.C04 with therapeutic potential as a monotherapy and, in combination.

Starpharma annual report and full-year financial results

On August 24, 2023 Starpharma (ASX: SPL, OTCQX: SPHRY) reported its full-year financial results for the year ended 30 June 2023 (Press release, Starpharma, AUG 24, 2023, View Source;mc_eid=bf52dd3418 [SID1234634654]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

Financial Results

Strong balance sheet with cash of $35.2 million at 30 June 2023. This excludes A$6.6M received from Mundipharma in August 2023, following the recent commercial settlement for VivaGel BV.
Reported loss down 3% to $15.6M (FY22: $16.2M).
Revenue down 14% to $4.2M (FY22: $4.9M).
Starpharma received a $7.1 million R&D tax incentive refund in December 2022, with an anticipated R&D tax incentive refund of $7.6 million expected in FY24.
Operational Highlights

Expanded partnerships with multinational pharmaceutical companies MSD and Genentech, exploring the application of DEP across several novel therapeutic modalities, including Antibody-Drug Conjugates (ADCs).
Generated additional clinical data across our three clinical DEP programs, including promising data for DEP cabazitaxel in patients with advanced prostate cancer, which were presented at the European Society of Medical Oncology (ESMO) (Free ESMO Whitepaper) Congress in Paris.
Completed recruitment of patients for all three in-house Phase 2 monotherapy clinical programs: DEP cabazitaxel, DEP docetaxel, and DEP irinotecan.
Launched VIRALEZE Antiviral Nasal Spray in Hong Kong and Macau through our partner Hengan Group, shortly after signing a new distribution agreement for these markets.
Commenced a post-market clinical study of VIRALEZE in patients with COVID-19 in the UK. The study has recruited ahead of target with more than 90% of the target participants now enrolled.
Advanced two new DEP pipeline products which demonstrated the unique benefits of the DEP platform in radiotheranostics and ADCs:
DEP HER2-zirconium, a radiodiagnostic for HER2-positive cancers, such as breast cancer and gastric cancer; and
HER2-targeted DEP SN38 ADC, a targeted ADC therapeutic, which outperformed leading ADC therapy Enhertu in a HER2+ human ovarian cancer model.
Dr Jackie Fairley, Starpharma CEO, commented, "Starpharma made significant progress across its portfolio during the 2023 financial year. Across our three Phase 2 DEP clinical programs, which have now completed recruitment in the monotherapy arms, we have seen encouraging efficacy signals and reductions in multiple clinically important side effects, compared to adverse events for conventional formulations of these drugs. Our trial clinicians continue to report improved patient experiences with DEP therapies. We were pleased to present data from the prostate cancer cohort of the DEP cabazitaxel trial at ESMO (Free ESMO Whitepaper) and look forward to releasing and presenting more data from our Phase 2 trials in Q3 CY23.

"We were delighted to expand our DEP partnerships with leading, global companies, MSD and Genentech, adding new programs of work, which are progressing well. Our antiviral nasal spray, VIRALEZE, was launched in Hong Kong and Macau, and new product registrations were achieved in Indonesia and Malaysia with further applications underway. Our post-market clinical study of VIRALEZE in people with COVID-19 is recruiting ahead of schedule, with more than 90% of participants enrolled and data expected soon after completion.

"Starpharma remains in a very strong financial position, with cash reserves of $35.2 million at 30 June 2023, and the subsequent receipt of A$6.6M in August 2023, from Mundipharma, following the signing of a settlement agreement related to VivaGel BV.

"Looking ahead, we have a number of exciting milestones, including results from our DEP oncology trials, multiple upcoming presentations at international oncology and radiotheranostics meetings, as well as results from our post-market VIRALEZE study. We also expect advances in our partner and preclinical DEP programs, as well as for VIRALEZE and VivaGel BV."

Key Activities
DEP Drug Delivery Programs

Starpharma’s Phase 2 clinical trial of DEP cabazitaxel completed the enrolment and treatment of patients, with 76 participants enrolled. Encouraging efficacy signals following treatment with DEP cabazitaxel have been observed, including significant tumour shrinkage and tumour biomarker reductions, in heavily pre-treated patients with advanced cancers, including prostate, ovarian, gastrooesophageal, cholangiocarcinoma and head and neck cancer. In September 2022, Starpharma presented promising results from the prostate cancer cohort at the European Society of Medical Oncology (ESMO) (Free ESMO Whitepaper) Congress. Starpharma expects to report the Phase 2 results from this trial in Q3 CY23, with partnering discussions ongoing.

The Phase 2 monotherapy arm of the DEP docetaxel trial also completed enrolment and treatment of patients. 50 patients were recruited and treated with DEP docetaxel in the monotherapy arm, and encouraging efficacy signals, including prolonged stable disease and significant tumour shrinkage, have been observed in heavily pre-treated patients with multiple cancer types, including pancreatic cancer, gastro-oesophageal cancer, and cholangiocarcinoma. Starpharma expects to report the Phase 2 results from this trial in Q3 CY23, with partnering discussions ongoing.

Starpharma also completed patient enrolment in the monotherapy arm of the Phase 2 clinical trial of DEP irinotecan, with 88 patients having been enrolled in the monotherapy arm. Encouraging results have been seen in patients with multiple cancer types, including colorectal, platinum-resistant ovarian, gastrointestinal, and breast cancer, with durable responses for up to 72 weeks. Starpharma also progressed the combination arms of the DEP irinotecan (5-FU/leucovorin) and DEP docetaxel (gemcitabine) Phase 2 trials, with final patient recruitment underway. The irinotecan plus 5-FU/leucovorin combination is a standard-of-care treatment regimen for colorectal cancer.

In parallel with completing these Phase 2 programs, Starpharma continued to build its pipeline of DEP assets, advancing the development of two promising products in DEP radiotheranostics and DEP ADCs. In June 2023, Starpharma announced that DEP HER2-zirconium, a HER2-targeted radiodiagnostic, demonstrated imaging benefits in a HER2+ breast cancer model. The demonstrated benefits included a favourable biodistribution profile, excellent imaging contrast between tumour and normal tissues, rapid uptake, and high levels of tumour accumulation. In addition, Starpharma announced the development of a HER2-targeted DEP SN38 ADC, which demonstrated significant anti-tumour activity and improved survival in a HER2-positive (HER2+) human ovarian cancer xenograft model, outperforming a leading HER2-ADC, Enhertu.

Starpharma’s partners include some of the world’s largest pharmaceutical companies, such as MSD, Genentech, Chase Sun and AstraZeneca. During the financial year, Starpharma expanded its DEP programs with MSD and Genentech to include new programs of work. Starpharma’s partnered programs apply the Company’s DEP platform technology to several novel therapeutic modalities, including Antibody-Drug Conjugates. In late July 2023, AstraZeneca announced it had made the decision to discontinue the development of AZD0466, following an internal review of its haematology portfolio. AstraZeneca confirmed that the asymptomatic adverse events leading to this decision were not related to the dendrimer component of AZD0466. Starpharma’s DEP License Agreement with AstraZeneca remains in effect. Starpharma maintains an active business development program for the DEP platform, with commercial discussions underway in a number of areas, including DEP radiotheranostics and DEP ADCs. The recently released positive data in both these areas feed into these discussions and will be showcased at upcoming international conferences.

VIRALEZE Antiviral Nasal Spray

During the financial year, Starpharma’s antiviral nasal spray, VIRALEZE, was launched in new markets, including Hong Kong and Macau, through an extensive network of retail stores, online, and other channels. The launch followed the signing of a sales and distribution agreement with Hengan Group and was supported by marketing activities. Hengan is based in China, listed on the Hong Kong Stock Exchange, has an annual turnover of ~A$4.5 billion and employs ~23,000 staff.

Marketing of VIRALEZE continued in multiple jurisdictions, including Hong Kong, Macau, Vietnam, the UK, and Europe. During the year, Starpharma expanded its e-commerce channels in the UK, making VIRALEZE available through a dedicated product website and Amazon UK. This year, Starpharma achieved registration for VIRALEZE in Malaysia and Indonesia, bringing the number of countries where VIRALEZE is registered to more than 35, and submitted regulatory applications in other jurisdictions. VIRALEZE is not approved for use or supply in Australia. The review by the Therapeutic Goods Agency (TGA) for the SPL7013 nasal spray as a medical device is ongoing.

Starpharma commenced a post-market clinical study of VIRALEZE in the UK in December 2022. The study will provide valuable clinical data on the antiviral performance of VIRALEZE in COVID-19-positive individuals. The study has recruited ahead of schedule, with more than 90% of participants enrolled to date. Starpharma presented new data on the efficacy of VIRALEZE against SARS-CoV-2 omicron infection in an animal challenge model at the international virology conference Respi DART in December 2022. These data, which were generated at Scripps Research in the US, showed that VIRALEZE was able to eliminate the SARS-CoV-2 omicron virus by more than 99.99% in the lung and trachea of animals that were exposed to the virus, even when VIRALEZE was administered after exposure.

VivaGel Portfolio

Starpharma’s VivaGel BV product continued to be marketed in multiple jurisdictions, including by Starpharma’s partner Aspen in Australia and New Zealand. Marketing campaigns by partners to build brand awareness and sales are ongoing, including for consumer and professional healthcare audiences. In August 2023, Starpharma announced it had negotiated a commercial settlement agreement with Mundipharma for VivaGel BV, which included a A$6.6M cash payment to Starpharma. Under the agreement, Starpharma also regained all commercial rights to VivaGel BV, enabling Starpharma to appoint new marketing partners, with commercial interest already expressed in the product. In the US, a formal dispute resolution process is ongoing with the Food and Drug Administration (FDA) for VivaGel BV. As part of this process, Starpharma has received extensive external advice, met the FDA
on multiple occasions, and made a number of submissions of data and analyses to the regulator. The Company is preparing to lodge a further submission to the FDA, including precedents of other FDA approvals, with the timing of lodgement governed by the publication and incorporation of relevant precedent information.

Starpharma’s VivaGel Condom continues to be marketed by Okamoto in Japan, with Okamoto also pursuing approvals in other Asian countries.

Corporate

Ms Zita Peach retired from the Board in November 2022 after 11 years. In February 2023, Starpharma welcomed medical oncologist and former senior executive Dr Russell Basser to the Board. Dr Basser has substantial expertise in international drug and vaccine development, having held multiple senior executive roles at CSL. In April 2023, Mr Justin Cahill joined Starpharma as Chief Financial Officer (CFO) and Company Secretary. Mr Cahill has extensive corporate finance and leadership experience in the biopharmaceutical, food, and agricultural sectors with several private and ASX-listed companies, including CSL. In February 2023, Starpharma appointed Ms Tracy Weimar as interim Company Secretary.

In June 2023, Dr Jackie Fairley advised the Board of her intention to retire as CEO in 2024 after 17 years. A search process is underway and Dr Fairley, the Board, and the senior executive team are working closely to ensure a seamless transition.

Financials

Starpharma concluded FY23 in a strong financial position with a cash balance of $35.2 million. Net operating cash outflows for the year were $13.5 million (FY22: $13.2 million). This excludes A$6.6M received from Mundipharma in August 2023 following the recent commercial settlement for VivaGel BV.

Revenue for FY23 was $4.2 million (FY22: $4.9 million), which included $2.9 million from VIRALEZE and VivaGel product sales, royalties, licensing revenue, and research revenue from commercial partners, as well as interest income of $1.3 million.

The FY23 loss after tax continued to trend downwards to $15.6 million (FY22: $16.2 million). Expenditure included investment in research and product development associated with the internal DEP drug delivery programs, including Starpharma’s clinical-stage products, DEP cabazitaxel, DEP docetaxel, DEP irinotecan, which have now largely completed recruitment, as well as DEP ADCs, and DEP radiotheranostics, and the post-market clinical study of VIRALEZE.

Starpharma received a $7.1 million R&D tax incentive refund in December 2022, with an anticipated R&D tax incentive refund of $7.6 million expected in FY24.