Milestone Pharmaceuticals to Present at Upcoming Investor Conferences

On November 14, 2019 Milestone Pharmaceuticals Inc. (Nasdaq: MIST) reported that Joseph G. Oliveto, President and Chief Executive Officer, will present at the following investor conferences (Press release, Milestone Pharmaceuticals, NOV 14, 2019, View Source [SID1234551337]):

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The Jefferies 2019 London Healthcare Conference on Thursday, November 21, 2019 at 3:20 p.m. Greenwich Mean Time (10:20 a.m. Eastern Time)
The Piper Jaffray 31st Annual Healthcare Conference in New York on Wednesday, December 4, 2019 at 3:30 p.m. Eastern Time
A live webcast of each presentation can be accessed in the News & Events section of Milestone’s website at www.milestonepharma.com. An archived replay of each webcast will be available on the same website for approximately 30 days following the presentation.

Seneca Biopharma Reports Third Quarter 2019 Fiscal Results

On November 14, 2019 Seneca Biopharma, Inc. (Nasdaq: SNCA), a clinical-stage biopharmaceutical company developing novel treatments for various diseases of high unmet medical need, reported its financial results for the three and nine months ended September 30, 2019 (Press release, Seneca Biopharma, NOV 14, 2019, View Source [SID1234551336]).

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RECENT HIGHLIGHTS & ACCOMPLISHMENTS:

Name change to Seneca Biopharma, Inc. (SNCA) in October 2019;
Signed non-binding term sheet for an exclusive license to a pipeline of monoclonal antibody product candidates for a range of auto-immune and other diseases;
Completed $7.5 million underwritten public offering; and
Regained compliance with the NASDAQ listing requirements.
"We are pleased at the progress we have made to reshape our company. Changing our name to Seneca Biopharma, Inc. is symbolic of our new focus and direction. Additionally, with our recently announced non-binding term sheet with Jiangsu QYuns Therapeutics Co., Ltd., we have accomplished one of our primary objectives in moving forward with the transformation of the Company" said Ken Carter, Executive Chairman of Seneca.

Financial Results for the Quarter Ended September 30, 2019

Research and Development Expenses: R&D expenses for the quarter ended September 30, 2019 decreased to $0.8 million versus the comparable period of 2018 of $0.9 million. The decrease reflects reduced clinical activities offset by increases in costs of identification and evaluation of strategic program opportunities.

R&D expenses for the nine months ended September 30, 2019 increased by $0.2 million, 7%, to $3.3 million from $3.1 million over the comparable period of 2018. This increase was primarily attributable to increases in costs of identification and evaluation of strategic program opportunities, a $0.5 million write-off related to an employee payable in connection with such employee’s termination, and partially offset by a decrease in clinical costs.

General and Administrative Expenses: G&A expenses for the quarter ended September 30, 2019 increased by $0.1 million to $1.3 million, or 10%, over the $1.2 million reflected in the comparable period of 2018. This increase primarily relates to an increase in non-cash compensation expense which was partially offset by a decrease in tax expense.

G&A expenses for the nine months ended September 30, 2019 decreased by $0.4 million to $3.2 million, or 13%, from $3.6 million reflected in the comparable period of 2018. This decrease is the result of general expense reduction efforts across multiple areas including consulting, outside services, tax and insurance expense as well as an increase in non-cash compensation expense.

Net Loss: Net loss for the quarter ended September 30, 2019 was $1.8 million, or $0.59 per share, compared to a loss of $1.8 million, or $2.41 per share, for the comparable period of 2018. Weighted average shares outstanding were 3.0 million shares at September 30, 2019 compared to 0.76 million shares at September 30, 2018.

Net loss for the nine months ended September 30, 2019 was $6.3 million, or $4.80 per share, compared to a loss of $4.6 million, or $6.08 per share, for the comparable period of 2018. Weighted average shares outstanding were 1.3 million shares at September 30, 2019 compared to 0.76 million shares at September 30, 2018.

All per share numbers have been retroactively adjusted for our 1-for-20 reverse stock split.

The net loss in the three and nine-month periods of 2018 were positively impacted by reductions in the derivative liabilities related to outstanding warrants reflected on the September 30, 2018 statement of operations of $0.2 and $1.8 million, respectively. The corresponding 2019 three- and nine-month periods also reflect reduced derivative liabilities with the impact reflected on the statement of operations in the amounts of $0.3 and $0.4 million, respectively.

Cash Position and Liquidity: At September 30, 2019, cash, cash equivalents and short-term investments were $7.3 million as compared to $5.8 million at December 31, 2018. The Company anticipates its existing cash, cash equivalents to fund its operations, based on its current operating plans, into the third quarter of 2020.

Medicenna Announces Presentations on MDNA55 Recurrent Glioblastoma Clinical Trial at the Annual Meeting of the Society of Neuro-Oncology

On November 14, 2019 Medicenna Therapeutics Corp. ("Medicenna" or "the Company") (TSX: MDNA,OTCQB: MDNAF), a clinical stage immuno-oncology company, reported that key opinion leaders, Dr. Sampson and Dr. Butowski, will present updated results from the Phase 2b clinical trial of MDNA55 for the treatment of recurrent glioblastoma ("rGBM") at the 24th Annual Meeting of the Society of Neuro-Oncology ("SNO") and 3rd Joint Conference of SNO and Society for CNS Interstitial Delivery of Therapeutics ("SNO-SCIDOT") to be held from November 20 to 24 at the JW Marriott Desert Ridge Resort in Phoenix, Arizona (Press release, Medicenna Therapeutics, NOV 14, 2019, View Source [SID1234551335]).

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The oral presentations will provide an update on efficacy, safety and data from the MDNA55 Phase 2b clinical trial in patients with rGBM, the most common and deadly form of brain cancer.

Details of the presentations are as follows:

Presenter: Dr. Nicholas Butowski, MD – Professor of Neurological Surgery and Director of Translational Research in Neuro-Oncology at The Helen Diller Family Comprehensive Cancer Center, University of California San Francisco
Title: Convection-Enhanced Delivery (CED) of MDNA55 in Adults with Recurrent Glioblastoma
Date/Time: Wednesday, November 20, 2019 at 3:10 PM MT
Room: Grand Saguaro East

Presenter: Dr. John Sampson, MD, PhD, MHSc, MBA – Robert and Gloria Wilkins Distinguished Professor and Chair of Neurosurgery, Department of Neurosurgery, Duke University School of Medicine
Title: Combating Recurrent Glioblastoma with MDNA55, an Interleukin-4 Receptor Targeted Immunotherapy, Through MRI-Guided Convective Delivery
Date/Time: Sunday, November 24, 2019 at 9:45 AM MT
Room: Grand Canyon 1 – 6

Invitation to Presentation of Sectra’s Six-month Interim Report on November 29, 2019

On November 14, 2019 The international medical imaging IT and cybersecurity company Sectra (STO: SECT B)reported that it will publish its interim report for the period May to October 2019 on November 29, 2019 (Press release, Sectra, NOV 14, 2019, View Source [SID1234551334]). Sectra invites analysts, investors, and the media to attend a teleconference/audiocast in conjunction with the publication of the report.

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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

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Publication of the interim report: 8:15 a.m. (CET) November 29, 2019

Presentation and audiocast: 10:00 a.m. (CET) November 29, 2019

To participate, follow online at investor.sectra.com/q2report2019 or call one of the following numbers five to ten minutes before the conference begins:

SE: +46850558356
UK: +443333009261
US: +18338230586

Sectra management will present the interim report and answer any questions. The presentation will be held in English and a recorded version will be available via investor.sectra.com/q2report2019 after the conference.

Approximately 30 minutes before the start, a PDF version of the presentation will be available for download.

Sectra’s financial report calendar

March 4, 2020 at 08:15 a.m.: Nine-month interim report
June 3, 2020 at 8:15 a.m.: Year-end report 2019/2020
Further information about Sectra’s financial events and interim reports: investor.sectra.com/events-and-presentations/

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To subscribe to financial reports, invitations, and information from Sectra via email, please fill in your contact information at investor.sectra.com/subscribe

Cardax Reports Q3 2019 Results

On November 14, 2019 Cardax, Inc. (OTCQB:CDXI) reported that results for the third quarter of 2019 (Press release, Cardax Pharmaceuticals, NOV 14, 2019, View Source [SID1234551333]). Highlights were as follows:

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CHASE Clinical Trial. On September 23, 2019, the Company announced results from the pre-specified interim review of its ongoing CHASE (Cardiovascular Health Astaxanthin Supplement Evaluation) clinical trial.

The CHASE clinical trial is a double-blind, randomized, placebo-controlled clinical trial evaluating the effect of the Company’s astaxanthin dietary supplement ZanthoSyn, on cardiovascular health, as measured by C-Reactive Protein or "CRP" levels over 12 weeks in up to 120 subjects with documented cardiovascular risk factors. Pre-specified secondary cardiovascular/inflammatory health markers, safety parameters, exploratory endpoints, and pre-specified sub-groups are also being assessed. The trial includes an optional open-label extension through 48 weeks.

The interim results were based on data from 40 subjects administered high dose ZanthoSyn (96 mg/day astaxanthin—48 mg twice a day), low dose ZanthoSyn (24 mg/day astaxanthin—12 mg twice a day), or placebo. The Company believes these encouraging findings provide:

Further mechanistic support for the Company’s astaxanthin pharmaceutical development program
Basis for additional patent filings
Support for the cardiovascular health benefits of ZanthoSyn*
View press release: Cardax Announces Interim Results from CHASE Clinical Trial, September 23, 2019

Intellectual Property. The Company filed additional patents to extend patent coverage in the U.S. and worldwide to 2039-2040, with such applications including coverage related to certain cardiovascular uses on the basis of the CHASE clinical trial results as well as coverage related to the composition of matter of CDX-101, the Company’s lead pharmaceutical candidate.

ZanthoSyn. Revenues rebounded in Q3 2019 with a more than five times increase compared to the previous quarter: $229,142 in Q3 2019 vs. $45,391 in Q2 2019. The rebound was driven by a return to normal inventory sell-in patterns, where "sell-in" is defined as wholesale orders of ZanthoSyn by General Nutrition Corporation ("GNC") less sales incentives, promotions, discounts, and refunds. Sell-through (retail sales of ZanthoSyn to GNC customers) also continued strong and the Company expects this trend to continue. ZanthoSyn is the top-selling product nationwide in GNC’s antioxidant category for 2019 year-to-date as well as the top-selling overall product in GNC’s Hawaii stores.

Financing. The Company raised $1,390,000 since the beginning of Q3 2019 to date, primarily via convertible notes, with the majority of this amount to automatically convert to equity upon a qualified financing of $5,000,000 or more. Net proceeds are being used for general working capital and to fund research, development, and clinical programs.

"We are very pleased with the encouraging CHASE trial interim results and our new patent filings. These milestones reflect the successful execution of key parts of our strategy to create value around our pharmaceutical development programs," said David G. Watumull, Cardax President and CEO. "On the consumer side of the business, the rebound in ZanthoSyn sales in Q3 2019 serves as an excellent foundation for Q4 2019 and Q1 2020."