Moleculin Announces Successful Completion of Pre-IND Meeting with the FDA

On September 9, 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 and viruses, reported that it successfully completed a pre-IND (Investigational New Drug) meeting with the U.S. Food and Drug Administration (FDA) regarding the development plan for Annamycin, including the clinical study design and dosing strategy for the initial phase 1b/2 protocol for soft tissue sarcomas with lung metastases (Press release, Moleculin, SEP 9, 2020, View Source [SID1234564802]).

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Moleculin submitted a proposed clinical protocol for FDA review entitled, "Phase 1b/2 Study of Liposomal Annamycin (Annamycin) in Subjects with Previously Treated Soft-Tissue Sarcomas with Pulmonary Metastases." The proposed study is an open-label, multicenter, single-arm, dose escalation and expansion study to evaluate single-agent Annamycin in up to 55 patients with soft tissue sarcoma (STS) with lung metastases for whom chemotherapy is considered appropriate. The primary objectives of the dose escalation phase are to evaluate the safety of Annamycin and identify the maximum tolerated dose (MTD) or the recommended Phase 2 dose (RP2D).

In summary, the FDA, among other items:

did not object to the proposed clinical study design while providing guidance on additional assessments

agreed the proposed dose escalation schedule appeared reasonable

commented regarding the consideration for including adolescents in oncology clinical trials

stated that a repeat dose toxicology study of 3 months is required before initiating a registration study

recommended an EOP1 meeting after completion of the RP2D.

"We are pleased to complete the pre-IND meeting with the FDA, and will move forward with our plans to file the IND by the end of 2020 and initiate a Phase 1b/2 trial of Annamycin for the treatment of soft tissue sarcomas metastasized to the lungs," said Wally Klemp, Chief Executive Officer of Moleculin. "We appreciate the FDA’s guidance as we endeavor to find a cure for certain cancers metastasized to the lungs."

Kaleido Biosciences to Present at Upcoming September Investor Conferences

On September 9, 2020 Kaleido Biosciences, Inc. (Nasdaq: KLDO), reported that Michael Bonney, Executive Chair, will participate in the following upcoming conferences in September (Press release, Kaleido Biosciences, SEP 9, 2020, View Source [SID1234564801]). Each conference will involve a fireside chat presentation.

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Event: Morgan Stanley 18th Annual Global Healthcare Conference
Date: Wednesday, Sept. 16, 2020
Time: 12:30 p.m. EDT

Event: Cantor 2020 Virtual Global Healthcare Conference
Date: Thursday, Sept. 17, 2020
Time: 3:20 p.m. EDT

A live webcast of each event will be available in the Investors & Media section of the Kaleido website at View Source Archived replays will be accessible following each event.

PHIO PHARMACEUTICALS TO PRESENT AT THE H.C. WAINWRIGHT 22ND ANNUAL GLOBAL INVESTMENT CONFERENCE

On September 9, 2020 Phio Pharmaceuticals Corp. (Nasdaq: PHIO), a biotechnology company developing the next generation of immuno-oncology therapeutics based on its proprietary self-delivering RNAi (INTASYL) therapeutic platform, reported that its chief executive officer, Dr. Gerrit Dispersyn, will present at the upcoming H.C. Wainwright 22nd Annual Global Investment Conference, held virtually this year from September 14 – 16, 2020 (Press release, Phio Pharmaceuticals, SEP 9, 2020, View Source [SID1234564800]).

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Dr. Dispersyn is scheduled to present on Wednesday, September 16th, at 11:30 a.m. ET. Interested parties may access a live webcast of the presentation at View Source

An archived version of the webcast and the slides used in the presentation will be made available on the "Investors – Events and Presentations" section of the Company’s website after the live event.

Oasmia Pharmaceutical AB (publ) Interim report for the period May 1 – July 31, 2020

On September 9, 2020 Oasmia Pharmaceutical AB (publ)reported that Interim report for the period May 1 – July 31, 2020 (Press release, Oasmia, SEP 9, 2020, View Source [SID1234564799])

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SIGNIFICANT EVENTS DURING THE FIRST QUARTER
Oasmia announced in May the outcome of a strategic review to deliver long-term, profitable growth as a specialty pharma company. As a result of the review, Oasmia will discontinue commercial manufacturing and implement cost reductions that will result in savings of MSEK 100 on an annual basis and a monthly burn rate of below MSEK 10.
An Extraordinary General Meeting in May elected existing Board member Anders Härfstrand as new Chairman of the Board and Birgit Stattin Norinder as new member of the Board. Jörgen Olsson, former Chairman of the Board, and Gunilla Öhman, former Board member, stepped down from the Board.
Oasmia signed in June a Phase 1b Trial Agreement with SAKK, the Swiss Group for Clinical Cancer Research, for evaluation of docetaxel micellar for the treatment of metastatic prostate cancer.
In July Oasmia’s partner Elevar Therapeutics and Tanner Pharma Group announced a global Named Patient Program to provide access to Apealea in areas outside of the United States.
The outbreak of COVID-19 and its effects around the world accelerated during the first quarter of the financial year. The pandemic has entailed heavily reduced access to health care providers and oncologists, which continues to have a profound negative impact on the marketing activities of the company.
SIGNIFICANT EVENTS AFTER THE REPORTING PERIOD
In August Oasmia appointed Peter Selin as Chief Business Officer.
Oasmia’s CFO Michael af Winklerfelt resigned from his role in August.
In September Oasmia’s Nomination Committee revised its proposal for the AGM regarding Board of Directors and Sven Rohmann notified that he is no longer available for re-election.
In September Oasmia appointed Fredrik Järrsten as Chief Financial Officer.
FIRST QUARTER: MAY 1, 2020 – JULY 31, 2020
Consolidated net sales amounted to TSEK 208 (182)
Operating income was TSEK -49,220 (-35,764)[3]
Net income after tax amounted to TSEK -53,105 (-39,783)[3]
Earnings per share was SEK -0.12 (-0.13)[3,4]
CEO’S COMMENTS
During the first quarter at Oasmia, we continued to work to deliver the strategic vision we set out following the announcement of the global strategic partnership with Elevar Therapeutics to commercialize our anti-cancer therapy Apealea.

Oasmia retains the rights to Apealea in the Nordic countries under the agreement with Elevar and is now making the product commercially available. The Covid-19 pandemic has inevitably impacted the ability of our medical scientific liaisons to meet oncologists during the quarter. An easing of lockdown restrictions will help resuming medical activities to return to more normal levels during the rest of the year.

Elevar entered into an agreement with Tanner Pharma Group in July to establish a named patient program that will facilitate patient access to Apealea in countries outside the US where it is not yet commercially available. The goal of the program is to assist cancer patients who have no alternative therapeutic options to get access to the drug. Apealea is the only cremophor-free product approved in Europe for use in combination with carboplatin for the treatment of adults with first relapse of platinum-sensitive epithelial ovarian cancer, primary peritoneal cancer and fallopian tube cancer. The initial target population for ovarian cancer is therefore patients with potential or previously established hypersensitivity reactions to currently used solubility enhancer containing paclitaxel formulations. We hope that this will make them particularly eligible to our XR-17 based paclitaxel formulation.

The collaboration with Elevar that started in 2020, as well as the transfer of all commercial manufacturing of Apealea to Baxter at the end of 2018, were important developments in realigning our growth strategy, enabling us to focus resources where they can bring the best return for shareholders.

The Board’s long-term vision is to build a cash flow-positive specialty pharmaceutical company. To help achieve this, we have implemented a strategic reorganization of Oasmia to focus on R&D and Business Development and to reduce unnecessary expenditure. With a proven technology in XR-17, a highly promising approved anti-cancer product, Apealea, and a global commercialisation agreement worth up to $678 million plus royalties, we are well positioned to grow through M&A and licensing deals for late-stage and marketed products. We will seek further opportunities to apply our proprietary XR-17 solubility-enhancing technology platform, primarily in oncology but also in other therapeutic areas. We are also looking at the potential to out-license the technology in non-core applications. We are already in the process of reviewing strategic options for our Animal Health business.

We will continue to drive the development of our pipeline of XR-17-based products and leverage the Company’s manufacturing expertise for R&D. Current promising lead programs include docetaxel micellar in metastatic prostate cancer. In June, we signed an agreement with the Swiss research group SAKK to conduct the first clinical trial of docetaxel micellar in advanced prostate cancer. Oasmia’s docetaxel micellar formulation is based on XR-17, which enables greater use of otherwise water-insoluble cancer drugs while reducing the side effects or need for additional medications associated with traditional solubility enhancers. In addition, we continue the assessment of XR-19, the dual encapsulation technology platform.

During the rest of 2020 we will continue to advance key areas of our growth strategy, including working closely with Elevar to deliver key milestones for Apealea and support efforts to identify the most appropriate commercial partners for the product in Europe and China. The appointment of Peter Selin as Chief Business Officer, announced a few weeks ago, together with our strong cash position, will be invaluable as we continue to pursue growth through M&A and in- and out-licensing opportunities that complement our technology and business model.

I look forward to keeping you updated on our progress. Please accept my thanks for your patience and continued support as we further transform Oasmia into a sustainable and profitable growth business with long-term potential. Above all, we are here to help patients to better manage their cancer diseases.

Clarity Pharmaceuticals Announces the US FDA Grants Rare Paediatric Disease Designation to 64Cu-SARTATE™, a diagnostic for the clinical management of neuroblastoma

On September 9, 2020 Clarity Pharmaceuticals, a clinical-stage radiopharmaceutical company focused on the treatment of serious disease, reported that the U.S. Food and Drug Administration (FDA) has granted Rare Paediatric Disease Designation (RPDD) to 64Cu-SARTATE, a diagnostic for the clinical management of neuroblastoma (Press release, Clarity Pharmaceuticals, SEP 9, 2020, View Source [SID1234564751]).

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Dr Alan Taylor, Clarity’s Executive Chairman, commented, "We are very excited to have received the RPDD status for the diagnostic application of SARTATE in children with neuroblastoma. This comes shortly after Clarity has been granted RPDD for the treatment of neuroblastoma with 67Cu-SARTATE for the therapeutic application, announced on the 3rd of June 2020."

The FDA defines a "rare paediatric disease" (RPD) as a serious or life-threatening disease primarily affecting individuals aged 18 years or younger that impacts fewer than 200,000 people in the United States. The program is intended to facilitate development of new drugs and biologics for the prevention and treatment of RPDs.

Neuroblastoma most often occurs in children younger than 5 years of age and presents when the tumour grows and causes symptoms. It is the most common type of cancer to be diagnosed in the first year of life and accounts for around 15% of paediatric cancer mortality.1 High-risk neuroblastoma accounts for approximately 45% of all neuroblastoma cases. Patients with high-risk neuroblastoma have the lowest 5-year survival rates at 40%-50%.2

Upon FDA marketing approval of 64Cu-SARTATE for neuroblastoma with RPD designation, Clarity would be eligible to receive a tradable Priority Review Voucher (PRV). The PRV shortens the FDA review period of a New Drug Application (NDA) for another product to an expedited period of six months, which is a huge benefit for drug developers. The voucher, if awarded, may be sold or transferred to another company. To date, PRVs have been sold for between US$67.5 million and US$350 million, with the most recent PRV being purchased by Merck from Lumos Pharma for a value of US$100 million in July 2020.3

"With 67Cu-SARTATE, a therapeutic for the clinical management of neuroblastoma, also having been awarded RPDD status4, Clarity may be eligible for two Priority Review Vouchers if both treatments get FDA approval," commented Dr Taylor.

"We have seen incredibly strong support from our collaborators and advisors in the development of SARTATE for neuroblastoma and are looking forward to the results from our US-based trial at the Memorial Sloan Kettering Cancer Centre5. It is evident that there is a large unmet need in the management and treatment of this devastating disease and we are aiming to improve outcomes for this important patient population with both the diagnostic and therapeutic applications of SARTATE" said Dr Taylor.