Neurotrope Announces Investor Update Conference Call

On May 26, 2020 Neurotrope, Inc. (Nasdaq: NTRP) reported that it will host an investor conference call and webcast to give an update on Bryostatin and the recently proposed merger between Neurotrope and Metuchen Pharmaceuticals, L.L.C. to form Petros Pharmaceuticals, Inc (Press release, Neurotrope, MAY 26, 2020, View Source [SID1234558536]). The investor call is scheduled for Thursday, May 28, 2020 at 11:00 AM ET .

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Conference Call and Webcast Information

The Neurotrope management team will host a conference call and webcast on Thursday, May 28, 2020, at 11:00 AM ET. The call can be accessed by dialing (833) 651-0992 (U.S. and Canada) or (918) 922-6081 (international), at least 10 minutes prior to the start of the call and providing the passcode 1870579.

The live, listen-only webcast of the conference call can be accessed by visiting the "Events & Presentations" page in the "Investors & Media" section of the Company’s website at www.neurotrope.com. An archived webcast will be available on the Company’s website approximately two hours after the event.

UPCOMING EVENTBolt invited to present:2020 Jefferies Virtual Healthcare ConferenceJune, 3, 2020

On May 27, 2020 Bolt Biotherapeutics, Inc., a private clinical-stage biotechnology company developing its Immune-Stimulating Antibody Conjugate (ISAC) platform technology to harness the power of the immune system to treat cancer, reported that Randall Schatzmann, Ph.D., chief executive officer of Bolt, will present a company overview at the 2020 Jefferies Virtual Healthcare Conference on Wednesday, June, 3, 2020 at 2:00 PM ET (Press release, Bolt Biotherapeutics, MAY 27, 2020, View Source [SID1234558533]).

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Qualigen Therapeutics Announces Merger Closing

On May 26, 2020 Qualigen Therapeutics, Inc. (NASDAQ: QLGN) (Qualigen or the Company) (formerly known as Ritter Pharmaceuticals, Inc. and formerly traded under the symbol RTTR), reported that it has completed its previously announced merger transaction with Qualigen, Inc., a company focused on the development of novel therapeutic products for the treatment of cancer and infectious diseases, as well as the worldwide sales of its flagship FastPack rapid diagnostic platform (Press release, Qualigen, MAY 26, 2020, View Source [SID1234558516]). The combined company will operate under the name Qualigen Therapeutics, Inc. pursuing the business of Qualigen, Inc., and the Company’s common stock will commence trading on the Nasdaq Capital Market at the open of trading today under the ticker symbol QLGN.

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"We are delighted to complete this transaction and extend a warm greeting to the former Ritter Pharmaceuticals shareholders," commented Michael Poirier, the new Chairman, President and Chief Executive Officer of the Company. "We look forward to developing Qualigen’s novel therapeutics pipeline for the treatment of cancer and infectious diseases, and expanding the reach and applications of our core FastPack diagnostic platform. The merger and concurrent financing provide Qualigen with enhanced resources and flexibility to pursue our corporate strategy and advance our programs."

In connection with the reverse merger transaction, a majority of the Company’s board of directors now consists of persons who had been directors of Qualigen, Inc., and all of the Company’s officers now consist of persons who had been officers of Qualigen, Inc.

Immediately prior to and in connection with the merger, Qualigen, Inc. completed a private placement of preferred stock to an institutional investor resulting in gross proceeds of approximately $4 million. In return, Qualigen, Inc. issued convertible preferred shares and warrants, which were exchanged in the merger for equivalent convertible preferred shares and warrants of the Company. These preferred shares and warrants contain a restriction from the holder owning more than 9.9% of the voting power of the Company, as well as anti-dilution and other customary investor protection provisions.

The Company issued common shares in the merger in exchange for all of Qualigen, Inc.’s common shares (including Qualigen, Inc. common shares into which all of Qualigen, Inc.’s outstanding preferred shares, excluding the preferred shares issued in the private placement, and almost all outstanding convertible notes had been converted immediately before the merger). A majority of the new Company common shares issued in the merger are subject to a six-month lockup agreement.

As a result of the merger and after taking into account the previously announced 1-for-25 reverse split of Ritter Pharmaceuticals common shares that became effective at the close of trading on May 22, 2020, the Company currently has a total of approximately 12.53 million shares of common stock outstanding, approximately 7.25 million additional shares of common stock potentially issuable upon the conversion of preferred stock and approximately 3.22 million outstanding common stock options and warrants. All legacy holders of Ritter Pharmaceuticals common shares remain stockholders of the Company, subject to the effect of the 1-for-25 reverse split of Ritter Pharmaceuticals common shares that became effective at the close of trading on May 22, 2020.

A Current Report on Form 8-K regarding the merger transaction and the financing will be filed with the Securities and Exchange Commission.

Qualigen Business Overview

Qualigen is a biotechnology company focused on developing novel products for the treatment and testing of cancer and infectious diseases. Its current commercial product is the FastPack rapid diagnostic testing system. This "Laboratory in a Pouch" is installed in physician offices, clinics and small hospitals around the world, and quickly detects diseases and medical conditions at the point-of-care. Since its inception almost 20 years ago, FastPack has generated more than $100 million in commercial sales. Qualigen’s worldwide distributor for FastPack is Sekisui Diagnostics, a subsidiary of a multibillion-dollar Japanese chemical and technology company. Sekisui owns approximately 15.8% of Qualigen’s outstanding common shares.

Qualigen’s therapeutic product pipeline includes pharmaceuticals being developed in collaboration with the University of Louisville and other partners, and an early stage proprietary blood cleansing system:

AS1411 and Gold Nanoparticle ALAN (AS1411-GNP): drug candidates that use a specialized segment of DNA, aptamers, to target and destroy tumor cells, enhance radiation therapy and aid in tumor scanning. Developed and previously placed into clinical trials for cancer therapeutics, the base AS1411 aptamer drug is now also being researched for halting replication of viral-based infectious diseases in humans. ALAN is expected to begin Phase I clinical trials for cancer in 2021.
RAS-F3: a small-molecule RAS oncogene protein-protein inhibitor that blocks RAS mutations directly, thereby inhibiting tumor formation. A RAS gene isoform (KRAS, HRAS or NRAS) is present in about one-fourth of all cancers, including pancreatic, colon and lung. Qualigen entered into a Sponsored Research Agreement with the University of Louisville for development of several small-molecule RAS Inhibitor drug candidates.
STARS blood cleansing system: using DNA aptamers and core, commercialized FastPack particle coating technology, STARS is being developed to remove tumor-produced compounds and viruses from a patient’s blood. Proof-of-concept has been established with in vitro testing.
Qualigen has 34 issued and pending patents worldwide to protect its technology, and has licensed rights to a further 10 patents. The Company also has 23 issued and pending patents worldwide held jointly with a third party. The Company’s new management team from Qualigen, Inc. has a proven track record of securing U.S. Food and Drug Administration (FDA) approvals and commercializing innovative technologies.

As previously disclosed, the Company does not intend to carry on Ritter Pharmaceuticals’ legacy business of developing therapeutic products that modulate the gut microbiome to treat gastrointestinal diseases. Holders of Company common stock as of immediately before the time the reverse stock split and merger were consummated will be entitled to receive a distribution of nontransferable contingent value rights (CVRs) from the Company. The CVRs will provide their holders with potential cash payment rights in the event of certain monetizations (if any and if ever) within a certain time period of this Ritter intellectual property.

Advisors

Ritter Pharmaceuticals’ financial advisor for the merger transaction was A.G.P./Alliance Global Partners. Reed Smith LLP served as legal counsel to Ritter Pharmaceuticals for the merger transaction and Stradling Yocca Carlson & Rauth served as legal counsel to Qualigen, Inc. for the merger transaction.

Conference Call

Qualigen’s management intends to hold a public business update conference call during the third quarter of 2020 to present an overview of the company and answer questions. Details of the call including instructions on how to participate will be announced prior to the date of the call.

Oncology Analytics Raises $28 Million Series C Financing Led by Baird Capital

On May 26, 2020 Oncology Analytics, a leading data analytics and technology-enabled services company dedicated to helping health plans, providers, and patients with solutions that are purpose-built for oncology, reported the completion of a Series C funding round of $28M (Press release, Oncology Analytics, MAY 26, 2020, View Source [SID1234558514]). Baird Capital led the round and joins existing investors Oak HC/FT, McKesson Ventures, and The Blue Venture Fund.

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The Series C financing will enable Oncology Analytics to expand its oncology-focused capabilities, accelerate real-world data and analytics solutions for health plans, and increase the market share of its technology-enabled utilization management solution. The company also announced that Michael Liang, partner at Baird Capital, has joined Oncology Analytics’ Board of Directors.

"The increasing cost of cancer care in the US has created an enormous burden for health plans and patients, which requires new thinking and a radical approach to solve," said Liang. "Oncology Analytics’ strategy, which puts data-science and real-world evidence at the center of the treatment decision-making process, demonstrates the type of innovative leadership needed in healthcare. Baird Capital looks forward to supporting Oncology Analytics to accelerate its mission."

"Oak HC/FT continues to be a strong advocate of the leadership team, strategy, and passion Oncology Analytics has for improving the lives of cancer patients," said Annie Lamont, managing partner, Oak HC/FT. "Over the past two years, Oncology Analytics has grown its customer portfolio by 400% and rapidly increased revenue. We are deeply committed to our partnership with Oncology Analytics and welcome Baird Capital to the team."

"It is incredibly humbling to have such a talented and experienced group of healthcare investors support our efforts to transform the oncology benefits landscape," said Rick Dean, CEO, Oncology Analytics. "We are delighted to welcome Michael and Baird Capital to the team, as I know this collaboration will accelerate our ability to bring value and innovation to our health plan customers."

Over the past decade, the oncology landscape has undergone dramatic changes, through an unprecedented number of new anti-cancer treatments brought to market, which have increased both the complexity and cost of care. By forging a deep connection between data science, analytics, and oncology expertise, Oncology Analytics provides health plans with extensive clinical insights to ensure that anti-cancer therapies are based on science and evidence-based protocols. Health plans are able to manage the total cost of cancer care while providing their members with treatment recommendations, which put them in the position to achieve the best possible outcome.

"Our health plan partners have told us that they need solutions that enable efficiency for their providers and themselves," Thomas Hawes, MD, managing director, The Blue Venture Fund. "Oncology Analytics removes a huge administrative burden on providers by enabling 100% of providers to submit their oncology prior authorization requests electronically through secure, cloud-based technology and receive instant approvals on evidence-based prescribing. We are proud to continue our support of the team as they continue to provide measurable value to health plans."

"McKesson Ventures is very impressed with the success Oncology Analytics has achieved since our initial investment, specifically, their ability to expand market share and increase the scale and depth of their technology," said Dave Schulte, managing director, McKesson Ventures.

Oncology Analytics’ Series C announcement comes during a period of tremendous growth and innovation for the company, which includes the increase of its prior authorization platform usage to 5 million health plan members. Oncology Analytics also recently announced a new customer partnership with Gateway Health, LLC, and program expansion with Humana, Inc.

Nordic Nanovector ASA: Results for the First Quarter 2020

On May 26, 2020 Nordic Nanovector ASA (OSE: NANO) reported its results for the first quarter 2020. A presentation by Nordic Nanovector’s senior management team will take place today via a webcast at 08:30 am CET (Press release, Nordic Nanovector, MAY 26, 2020, View Source [SID1234558513]). A link to the webcast and a presentation is available from the company’s homepage (www.nordicnanovector.com).

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Lars Nieba, interim CEO of Nordic Nanovector, said: "Despite a number of significant challenges, the new senior management team together with the Board and all our employees have moved decisively to conduct a thorough strategic review and to implement an action plan based on its conclusions. With a clear focus on PARADIGME and a cash runway into 2021, I believe we are well placed to demonstrate and deliver the value of Betalutin to patients and to our shareholders."

Q1’20 Highlights

Dr Lars Nieba appointed as interim Chief Executive Officer
Dr Dominic Smethurst appointed as interim Chief Medical Officer
Pivotal Phase 2b PARADIGME trial of Betalutin in 3rd-line follicular lymphoma (3L FL) progressing
COVID-19 has had a negative impact on PARADIGME during H1’2020
51 patients enrolled as of May 25th, 2020
Initiated strategic review with focus on advancing PARADIGME and extending cash runway into 2021
Events after Q1’20

Strategic review completed: clinical development strategy revised, and cost-saving initiatives implemented
FDA meeting sought to discuss PARADIGME protocol amendments designed to enlarge eligible patient population and increase rate of enrolment
Enrolment timelines for PARADIGME to be updated once FDA feedback is received and when there is more clarity on the impact created by COVID-19
Planned restructuring completed
Malene Brondberg appointed as Chief Financial Officer
Corporate and personnel reorganisation implemented
Headcount reduced by approx. 20%
Cost savings of approx. NOK 35 million in connection with the restructuring on an annual basis
Betalutin recommended for Orphan Drug Designation in the European Union for Marginal Zone Lymphoma (MZL)
Financial Highlights

(Figures in brackets = same period 2019 unless otherwise stated)

Revenues for the first quarter amounted to NOK 0.0 million (NOK 0.0 million)
Total operating expenses for the first quarter were NOK 125.9 million (NOK 90.0 million)
Comprehensive loss for the first quarter amounted to NOK 91.7 million (loss of NOK 91.6 million)
Cash and cash equivalents amounted to NOK 384.3 million at the end of March 2020, compared to NOK 470.8 million at the end of December 2019
Outlook

The company continues to target the readout of top line data from PARADIGME in 2021. However, due to uncertainties created by the current COVID-19 situation, there is a need to review the timeline for the enrolment of PARADIGME, which previously was guided for H2’2020. Updated timelines for PARADIGME are expected to be provided once there is more clarity on the impact of COVID-19 and when all the relevant regulatory feedback has been received.

Nordic Nanovector is fully committed to ensuring that PARADIGME has the best chance of success and the proposed protocol amendments are an important part of this. Following FDA feedback, the company intends to seek approval for these amendments at an individual country level and begin their implementation as they are approved.

The company believes that the improvements it has made to the conduct of PARADIGME puts it in a strong position to improve the rate of patient enrolment once COVID-19 restrictions are eased.

The steps the company has taken to conserve cash, including reducing headcount and pausing certain clinical trials, will extend the cash runway into 2021. The company expects to see the impact of these cost-saving initiatives emerge over the remainder of this year.

Following the comprehensive strategic review carried out by the new management team, the company believes it is now in a much-improved position to deliver the pivotal results from PARADIGME in a timely manner. This is a key milestone for Nordic Nanovector as the company seeks to bring this exciting new targeted NHL treatment to patients and maximise the value of Betalutin.