Annual report and full year financial results

On August 27, 2020 Starpharma (ASX: SPL, OTCQX: SPHRY) reported that financial results for the year ended 30 June 2020 (Press release, Starpharma, AUG 27, 2020, View Source [SID1234564098]).

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Financial Results

Cash position at 30 June 2020 of $30.1M
Net cash burn[1] of $11.2M (FY19: $10.1M)
Total revenue and other income of $7.1M (FY19: $2.7M), an increase of 162% compared to the prior year
Reported loss of $14.7M (FY19: $14.3M)
Receipt of $4.9M R&D tax incentive
Key activities

AstraZeneca commenced phase 1 trial for its first DEP product, AZD0466, and triggered a US$3 million milestone payment to Starpharma;
DEP irinotecan phase 1 trial commenced and was completed successfully with encouraging efficacy signals observed, and progressed to a phase 2 trial;
DEP cabazitaxel phase 1 trial was completed successfully with encouraging efficacy signals observed, and progressed to a phase 2 trial;
Starpharma’s internal clinical DEP trials for DEP docetaxel, DEP cabazitaxel and DEP irinotecan progressed well with all three assets now in phase 2 trials; encouraging efficacy signals were observed in each trial and multiple new sites opened;
DEP docetaxel + gemcitabine clinical combination study commenced following ethics committee and regulatory approvals;
VivaGel BV was launched in the UK and in Central and Eastern European countries, by Mundipharma under the Betadine brand; First Asian regulatory approvals were granted and VivaGel BV was launched in South East Asia; VivaGel BV achieved product sales and royalties of $1.5 million;
VivaGel BV achieved #1 ranking in topical BV treatment in Australia, and product roll-out continued in Australia under the brand name Fleurstat BVgel, and Aspen launched the product in New Zealand;
SPL7013 was tested and found to have significant activity against SARS-CoV-2, the coronavirus that causes COVID-19. Significant progress was made with product development for a nasal spray;
Development of a DEP radiotherapy product, DEP lutetium, opening up a new opportunity for the application of the DEP platform;
Signed a new DEP partnership with leading Chinese Pharmaceutical company Tianjin Chase Sun Pharmaceutical Co., Ltd, in a new therapeutic area (anti-infectives), with potential for additional programs in other therapeutic areas;
DEP irinotecan in combination with immuno-oncology (IO) showed superior anti-tumour activity and significant survival benefit compared to IO alone in two human colorectal cancer models;
Impressive data were reported for DEP irinotecan, alone and in combination with Lynparza, in a refractory human colon cancer model;
DEP gemcitabine demonstrated significantly enhanced anti-tumour activity compared with Gemzar (gemcitabine) in a human pancreatic cancer model;
A novel DEP HER-2 Targeted ADC (Antibody Drug Conjugate) conjugate demonstrated significant tumour regression and 100% survival in a preclinical human ovarian cancer model;
Continued to actively pursue US FDA approval of VivaGel BV including progressing a detailed administrative review process with the agency;
Expansion of Okamoto’s licence for the VivaGel condom in 11 further Asian countries (in addition to Japan);
Achieved EU approval for the VivaGel condom, and Lifestyles commenced marketing preparations for launch in Europe;
Advanced arrangements with potential partners of new Targeted (ADC) and non-ADC DEP programs;
Signed a new DEP partnered program with an existing partner in a novel area of cancer therapeutics, and progressed DEP program discussions with two further major pharmaceutical companies;
AACR (American Association for Cancer Research) Annual Meeting 2020 featured five posters based on Starpharma’s DEP products; and
TGA licence granted to Starpharma to manufacture DEP active pharmaceutical ingredient in-house for clinical trial purposes.
Starpharma concluded the year in a strong financial position with a cash balance of $30.1 million. Revenues for the year totalled $6.6 million including a US$3 million AstraZeneca milestone payment and $1.5 million for VivaGel product sales and royalties. The net loss after tax for the year was $14.7 million, 3% higher than the previous year due to increased development expenses associated with the company’s expanding clinical product portfolio, which now includes three phase 2 assets.

Starpharma CEO, Dr Jackie Fairley, commented: "The past year has been an extraordinary period for all of us. While COVID-19 has impacted companies around the world, Starpharma was able to achieve a number of important milestones during the year, including: significant progress with our internal clinical-stage DEP assets with three products now in phase 2; advancing multiple new development programs, including in antivirals and radiotherapy; in addition to several product launches of VivaGel BV in the UK, Europe and Asia".

Dr Fairley added: "As the pandemic emerged we also identified an opportunity for a preventative SPL7013 COVID-19 nasal spray. We already knew SPL7013 has broad spectrum antiviral activity, and undertook further testing which established it has significant activity against SARS-CoV-2. In a short period of time we have been able to develop nasal formulations, select a manufacturer and appropriate device components, and have undertaken pilot manufacture. We have also held discussions with regulators and confirmed a rapid development pathway. Feedback from key opinion leaders confirms that a SPL7013 antiviral nasal spray could be an important addition in preventing the transmission of COVID-19 and complementing vaccine-based strategies".

"One of several DEP milestones for the year included the commencement of AstraZeneca’s phase 1 trial for its first DEP product, AZD0466. In our internal DEP portfolio, we continued to advance our three clinical-stage DEP assets, including initiating a new combination study for DEP docetaxel; moving DEP cabazitaxel to phase 2; and successfully completing phase 1 for DEP irinotecan, ahead of schedule. We also made some important additions to our preclinical DEP pipeline with our first radiopharmaceutical, DEP lutetium, DEP gemcitabine and a novel HER-2 Targeted DEP (ADC)."

"In the year ahead, we will continue to advance our clinical DEP assets and expand our portfolio by moving up our preclinical programs and explore value-adding combinations to increase the market opportunities. Starpharma is well positioned for further growth as we achieve further approvals and launches in our VivaGel portfolio, as well as accelerating the development of our COVID-19 nasal spray.", concluded Dr Fairley.

Starpharma has published a standalone ESG (Environment, Social & Governance) Report which is available at View Source

Download ASX Announcement: Starpharma annual report and full year financial results (PDF, 6MB)

[1] Net cash burn is considered a non-IFRS value and has not been audited in accordance with Australian Accounting Standards. Net cash burn is calculated by the movement in cash and cash equivalents from 30 June 2019 to 30 June 2020.

PRESS RELEASE: Biognosys Announces Nature Communications Publication in Collaboration with ETH Zurich, Bayer, and BASF

On August 27, 2020 Biognosys reported the publication of new research findings in Nature Communications on the utility of its LiP technology and workflow for drug target identification (Press release, Biognosys, AUG 27, 2020, View Source [SID1234564095]). The publication, entitled "A Machine-Learning-Based Chemoproteomic Approach to Identify Drug Targets and Binding Sites in Complex Proteomes", is co-authored by collaborators from ETH Zurich, Biognosys, Bayer and BASF.

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In this publication, we present a novel chemoproteomic workflow combining LiP and machine learning-based data analysis. This next-generation proteomics approach enables the identification of small molecule drug targets in complex proteomes and the analysis of their binding properties across species and drug target classes.

Oliver Rinner, Chief Executive Officer of Biognosys, comments: "Understanding a compound’s mechanism of action remains a major challenge in drug development. This publication is a testimony to our commitment to support our pharma and biotech partners with unique applications for more efficient drug discovery."

Lukas Reiter, Chief Technology Officer, states: "Biognosys’ quantitative proteomics technology based on data independent acquisition (DIA) is a perfect fit for the LiP technology. This combined workflow enabled us to develop a target deconvolution approach for human cell lines."

Prof. Dr. Paola Picotti, Associate Professor in Molecular Systems Biology and head of the Picotti group at ETH Zurich, and Scientific Advisor for Biognosys, says: "With the LiP approach, we can now also identify compound-binding in very complex mammalian cell systems with high confidence. In addition, we get information on binding affinity, which helps us to prioritize targets for follow-up studies."

Thomas Knobloch, Laboratory Manager at Bayer CropScience, adds: "The LIP technology is a very valuable tool to identify target and off-target of novel compounds whatever the organism and to support the process of target deconvolution in early phase research."

Earlier this year, Biognosys published research findings demonstrating the utility of LiP-based proteomics for drug discovery at the US Human Proteome (HUPO) Conference and the American Association for Cancer Research (AACR) (Free AACR Whitepaper) Annual Meeting.

About Limited Proteolysis (LiP):
The Limited Proteolysis technology coupled to next-generation quantitative mass spectrometry is a novel approach that enables the unbiased and proteome-wide profiling of protein changes resulting from a variety of stimuli such as heat shock, protein-protein interactions, compound binding, and posttranslational modifications.

Invented by the group of Prof. Paola Picotti at ETH Zurich, this patented technology is exclusively licensed to and co-developed by Biognosys to support pharma and biotech partners with contract research services for drug discovery and development. Biognosys already offers a LiP-technology based target deconvolution application and is developing additional, machine-learning-based applications for target validation.

Ascendis Pharma A/S Reports Second Quarter 2020 Financial Results and Announces New Data from the Four-Week, Fixed Dose, Double-Blind Portion of the PaTH Forward Trial

On August 27, 2020 Ascendis Pharma A/S (Nasdaq: ASND), a biopharmaceutical company that utilizes its innovative TransCon technologies to address unmet medical needs, reported new data from PaTH Forward and financial results for the quarter ended June 30, 2020 (Press release, Ascendis Pharma, AUG 27, 2020, View Source [SID1234564094]).

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"We are executing across the globe on all elements of our Vision 3×3, including preparation for the expected U.S. launch for TransCon hGH following submission of our Biologics License Application (BLA) to the U.S. Food and Drug Administration (FDA) in June, and preparing to submit the Marketing Authorisation Application (MAA) to the European Medicines Agency (EMA) for TransCon hGH in Europe planned for third quarter," said Jan Mikkelsen, Ascendis Pharma’s President and Chief Executive Officer.

Mr. Mikkelsen continued, "Additionally, with today’s data release, we have, for the first time in a randomized, double-blind, placebo-controlled trial, demonstrated that a therapy for hypoparathyroidism (HP) may have a significant impact on improving quality of life for people living with HP compared to the standard of care. Our new data showed that TransCon PTH demonstrated a statistically significant1 and clinically meaningful impact on the SF-36 Health Survey (SF-36), a quality of life assessment tool validated to measure functional health and well being compared to placebo.2 Analysis of these exploratory endpoints, combined with expected findings from our proprietary patient reported outcome instrument, called Hypoparathyroidism Patient Experience Scale (HPES), will support the emerging body of evidence that TransCon PTH may function as a hormone replacement therapy and make a meaningful difference in improving the lives of people with HP."

Corporate Highlights & Progress

Submitted a BLA for TransCon hGH for pediatric growth hormone deficiency to the FDA on June 25, 2020.
In July, received approval of its proposed Paediatric Investigation Plan covering ages 6 months to less than 18 years of age from EMA for TransCon hGH and remain on track for a planned third quarter 2020 MAA submission to the EMA for pediatric growth hormone deficiency.
Today announced new data on exploratory endpoints from the four-week fixed dose, blinded portion of PaTH Forward, a global phase 2 trial evaluating the safety, tolerability and efficacy of TransCon PTH, an investigational long-acting prodrug of parathyroid hormone (PTH), in adult subjects with hypoparathyroidism. Data on TransCon PTH from the validated SF-36 quality-of-life instrument showed a statistically significant improvement related to both the physical (LS mean difference=5.2; p=0.013) and mental (LS mean difference=9.8; p=0.0003) components of the measure compared to placebo.1 Importantly, the results were consistent with a clinically meaningful improvement in functional health and well being for subjects receiving TransCon PTH as compared with placebo after four weeks.2 Detailed results are included in the company’s investor presentation which can be found on the company’s website at www.ascendispharma.com. The company plans to present additional data and analyses from the PaTH Forward trial four-week results at upcoming medical conferences, anticipates announcing the six-month data from the open-label extension portion of the PaTH Forward Trial during the third quarter and is preparing to submit regulatory filings to initiate a phase 3 trial in the fourth quarter.
In July, received orphan designation by the European Commission (EC) for TransCon C-Type Natriuretic Peptide (CNP), an investigational long-acting prodrug of CNP in development as a therapy for achondroplasia, the most common form of dwarfism.3
Presented preclinical data for TransCon IL-2 β/γ, an oncology product candidate designed to provide sustained systemic release of a receptor-biased IL-2 (IL-2 β/γ), at the American Association of Cancer Research (AACR) (Free AACR Whitepaper) Virtual Annual Meeting II. Results showed that TransCon IL-2 β/γ demonstrated a long in vivo half-life of approximately 32 hours, expected to support potential dosing of every three weeks in patients.4
After the end of the second quarter, the company announced the completion of its underwritten public offering of 4,859,154 American Depositary Shares ("ADSs"). Net proceeds from this offering in July 2020 were approximately $654.7 million, or approximately €580.7 million based on exchange rates on the date of the closing.
Ended the second quarter 2020 with cash, cash equivalents and marketable securities totaling €471.6 million, excluding the net proceeds from the July 2020 equity offering.
Second Quarter 2020 Financial Results

For the second quarter, Ascendis Pharma reported a net loss of €94.9 million, or €1.97 per share (basic and diluted) compared to a net loss of €58.9 million, or €1.25 per share (basic and diluted) for the same period in 2019.

Revenue for the second quarter was €1.4 million compared to €3.2 million in the same quarter of 2019. The decrease was due to a lower amount of license and service revenue being recognized from the company’s strategic investment in VISEN Pharmaceuticals.

Research and development (R&D) costs for the second quarter were €63.6 million compared to €43.8 million during the same period in 2019. Higher R&D costs in 2020 reflect an increase in personnel-related costs, overhead costs allocated to R&D, and the continued progress in development of the company’s product candidates.

Selling, general and administrative (SG&A) expenses for the second quarter were €20.8 million compared to €11.0 million during the same period in 2019. The increase is primarily due to additional personnel-related costs, higher IT and other site costs, and continued build out of the company’s commercial capabilities.

As of June 30, 2020, Ascendis Pharma had cash, cash equivalents and marketable securities totaling €471.6 million compared to €534.4 million as of March 31, 2020. As of June 30, 2020, Ascendis Pharma had 48,345,782 ordinary shares outstanding.

Conference Call and Webcast information

Ascendis Pharma will host a conference call and webcast today at 4:30 p.m. Eastern Time (ET) to discuss its second quarter 2020 financial results. Details include:

A live webcast of the conference call will be available on the Investors and News section of the Ascendis Pharma website at www.ascendispharma.com. A webcast replay will also be available on this website shortly after conclusion of the event for 30 days.

About Ascendis Pharma’s Pipeline

Ascendis Pharma currently has three product candidates in clinical development in rare endocrine diseases:

TransCon hGH (lonapegsomatropin), an investigational long-acting prodrug of somatropin (human growth hormone or hGH) that releases somatropin with the identical amino acid sequence and size as daily growth hormone, in phase 3 development as a once-weekly treatment for growth hormone deficiency (GHD).
TransCon PTH, an investigational long-acting prodrug of parathyroid hormone (PTH) in phase 2 development as a once-daily replacement therapy for hypoparathyroidism (HP) designed to replace PTH at physiologic levels for 24 hours every day, and address both short-term symptoms and long-term complications of the disease.
TransCon CNP, an investigational long-acting prodrug of C-type natriuretic peptide (CNP) in phase 2 development as a therapy for children with achondroplasia (ACH), the most common form of dwarfism3, for which there is no FDA-approved treatment5. TransCon CNP is designed to provide continuous exposure of CNP at safe, therapeutic levels via a single, weekly subcutaneous dose.
Additionally, the company has established oncology as its second therapeutic area of focus and plans to submit an IND or similar in the fourth quarter of 2020 for TransCon TLR7/8 Agonist, the company’s first oncology product candidate.

Advaxis to Present Corporate Overview at the LD Micro 500 Virtual Conference

On August 27, 2020 Advaxis, Inc. (Nasdaq: ADXS), a clinical-stage biotechnology company focused on the development and commercialization of immunotherapy products, reported that Kenneth A. Berlin, President and Chief Executive Officer of Advaxis, will present a corporate overview at the LD Micro 500 Virtual Conference, being held virtually September 1 – 4, 2020 (Press release, Advaxis, AUG 27, 2020, https://ir.advaxis.com/news-releases/news-release-details/advaxis-present-corporate-overview-ld-micro-500-virtual [SID1234564092]).

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Presentation Information:
Date: Wednesday, September 2nd
Time: 3:40 pm ET
Webcast: View Source

Moleculin to Present at LD Micro 500 Virtual Investor Conference

On August 27, 2020 Moleculin Biotech, Inc., (Nasdaq: MBRX) ("Moleculin" or the "Company"), a clinical stage pharmaceutical company with a broad portfolio of drug candidates targeting highly resistant tumors, reported that Walter Klemp, Chairman and Chief Executive Officer, will present at the LD Micro 500 Virtual Investor Conference being held virtually on Tuesday, September 1st, at 4:40pm ET (Press release, Moleculin, AUG 27, 2020, View Source [SID1234564091]).

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Moleculin Biotech, Inc. is a clinical stage pharmaceutical company focused on the development of a broad portfolio of oncology drug candidates for the treatment of highly resistant tumors. (PRNewsfoto/Moleculin Biotech, Inc.)

Details of the presentation are below:

Event:

LD Micro 500 Virtual Investor Conference

Date:

September 1st, 2020

Time:

4:40pm ET

Link:

View Source

Additionally, the Company will hold 1-on-1 virtual investor meetings at the conference. Investors attending the conference virtually who are interested in meeting with Company management should contact their LD Micro representatives.