Humanigen to Present at the BTIG Virtual Biotechnology Conference 2020

On August 5, 2020 Humanigen, Inc., (HGEN) ("Humanigen"), reported that Cameron Durrant, MD, MBA, Chief Executive Officer and Dale Chappell, MD, MBA, Chief Scientific Officer of Humanigen will present a company overview and business update at the BTIG Virtual Biotechnology Conference 2020 on Tuesday, August 11th, 2020 at 2:00 pm Eastern Time (Press release, Humanigen, AUG 5, 2020, View Source [SID1234562949]). The conference is being held in a virtual format.

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A live webcast of the event can be accessed at View Source

An archived replay of the event will be available on the Company website for 30 days following the event.

Rocket Pharmaceuticals Reports Second Quarter 2020 Financial Results and Highlights Recent Progress

On August 5, 2020 Rocket Pharmaceuticals, Inc. (NASDAQ: RCKT) ("Rocket"), a clinical-stage company advancing an integrated and sustainable pipeline of genetic therapies for rare childhood disorders, reported financial results for the quarter that ended June 30, 2020, along with an update on the Company’s key pipeline developments, business operations and upcoming milestones (Press release, Rocket Pharmaceuticals, AUG 5, 2020, View Source [SID1234562948]).

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"During this quarter, I am pleased to announce we continued to build pipeline momentum with positive data readouts and significant clinical trial progress," said Gaurav Shah, M.D., Chief Executive Officer and President of Rocket. "We continued to enroll patients in our FA, LAD-I and PKD trials, and received FDA clearance of our IND for IMO. In addition, we presented positive data demonstrating sustained efficacy for both RP-L102 for FA and RP-L201 for LAD-I at ASGCT (Free ASGCT Whitepaper). With the continued buildout of our manufacturing facility, we anticipate GMP clinical material produced in 2021. With steady commitment and dedication, we remain focused on establishing a truly integrated and industry-leading multi-platform gene therapy approach aimed at improving and saving lives."

Dr. Shah continued, "Our progress comes amidst the backdrop of COVID-19, which continues to affect the lives of millions. As members of the healthcare community, we are committed to continuing to operate with a sense of responsibility to our employees and patients as we advance our pipeline aimed at addressing so many devastating rare genetic disorders. We want to also applaud the relentless work of our partners, patients and healthcare communities who skillfully navigate and respond to this pandemic with passion and care."

Key Pipelines and Operational Updates

Phase 1 clinical trial of RP-A501 for the treatment of Danon Disease continues to progress. Rocket has been cleared by the U.S. Food and Drug Administration (FDA) and the Independent Data Safety Monitoring Committee (IDSMC) to move to the higher dose cohort of the study. The first patient in this cohort is expected to be treated in the third quarter, and preliminary Danon data is anticipated in the fourth quarter.
Positive clinical updates for the Company’s Fanconi Anemia (FA) and Leukocyte Adhesion Deficiency-I (LAD-I) programs presented at the American Society of Gene & Cellular Therapy (ASGCT) (Free ASGCT Whitepaper) meeting. At the virtual ASGCT (Free ASGCT Whitepaper) conference, Rocket presented longer-term data from the FANCOLEN-I study of RP-L102 "Process A" for FA. Patients followed for a year or more after treatment with RP-L102 "Process A" continued to demonstrate durable engraftment and hematologic correction, without the use of pre-treatment conditioning regimens. Updates on FA "Process B" data are expected in the fourth quarter. In Rocket’s Phase 1/2 study of RP-L201 for the treatment of severe LAD-I, the first patient treated with RP-L201 demonstrated an increase in CD18 expression from less than 1% to 45%, sustained over six months. These results lend further support to the applicability of "Process B" across the lentiviral portfolio. Enrollment is now complete in the Phase 1 portion of the study, and Rocket expects to move to Phase 2 in the fourth quarter. Additional LAD-I data are on track for the fourth quarter.
First patient treated in the Phase 1 Trial of RP-L301 for Pyruvate Kinase Deficiency (PKD). PKD represents the Company’s largest lentiviral program. The trial is designed to assess safety, tolerability and preliminary efficacy of RP-L301 for the treatment of PKD. Preliminary data is anticipated in the fourth quarter.
Global Phase 1 trial of RP-L401 for Infantile Malignant Osteopetrosis (IMO) initiates enrollment. The Company received Investigational New Drug (IND) application approval of RP-L401 at the end of the second quarter. The trial is designed to assess the safety, tolerability and preliminary efficacy of RP-L401.
Continued focus on supporting the patient community by serving as a pivotal resource for patient education during the COVID-19 pandemic. Throughout the quarter, as patients were faced with significant difficulties presented by the pandemic, the Rocket team made it a priority to connect with the community, share updates and host a variety of programs and events to support patients through this critical time. In addition to hosting multiple community Q&A sessions, the Rocket team and its partners participated in the 2020 Fanconi Anemia Family Meeting, hosted by the Fanconi Anemia Research Fund (FARF) where the latest FA data was presented, and a Q&A session was held for the patient community. More recently, Rocket organized two virtual sessions for patients with Danon Disease and their families. The first virtual event was focused on addressing the community’s concerns around COVID-19. The second event brought together patients with Danon Disease, their families and experts in the field to discuss current treatment options, the present state of research, the development of new treatments and ongoing clinical trials.
Rocket strengthens its balance sheet by extending the maturity of the existing convertible notes. Rocket extended the maturity of the 5.75% convertible notes due 2021. The Company conducted a second exchange offering and successfully exchanged an additional $7.5 million of the outstanding $12.65 million convertible notes. The new notes, with an aggregate principal amount of $46.85 million, will mature on August 1, 2022 and have an interest payment of 6.25% per annum. The remainder of the notes will retain the existing maturity date and interest payment.
Anticipated Milestones

FA (RP-L102)
Preliminary "Process B" data (4Q)
Phase 2 "Process B" data (2021)
Danon Disease (RP-A501)
First patient treatment in higher dose (3Q)
Preliminary Phase 1 data (4Q)
Phase 1 longer-term data (2021)
Phase 2 study initiation (2021)
LAD-I (RP-L201)
Initiate Phase 2 study (4Q)
Phase 1 data update (4Q)
Phase 2 data (2021)
PKD (RP-L301)
Preliminary Phase 1 data (4Q)
Longer-term Phase 1 data (2021)
Phase 2 study initiation (2021)
IMO (RP-L401)
Initiation of clinical study (4Q)
Phase 1 data (2021)
Phase 2 study initiation (2021)
Upcoming Investor Conferences

Citi’s 15th Annual BioPharma Virtual Conference, September 9-10, 2020
Morgan Stanley 18th Annual Global Healthcare Virtual Conference, September 14-18, 2020
Second Quarter Financial Results

Cash position. Cash, cash equivalents and investments as of June 30, 2020 were $249.8 million.
Debt. Our balance sheet includes $52.0 million of fully convertible notes.
R&D expenses. Research and development expenses were $16.7 million for the three months ended June 30, 2020, compared to $14.0 million for the three months ended June 30, 2019, due to an increase in compensation and benefits expense due to increased R&D headcount, and an increase in manufacturing and development costs.
G&A expenses. General and administrative expenses were $6.8 million for the three months ended June 30, 2020, compared to $4.4 million for the three months ended June 30, 2019, due to an increase in non-cash stock compensation expense and an increase in compensation and benefits expense due to increased G&A headcount.
Net loss. Net loss was $25.0 million or $0.45 per share (basic and diluted) for the three months ended June 30, 2020, compared to $18.7 million or $0.38 per share (basic and diluted) for the three months ended June 30, 2019.
Shares outstanding. 55,170,003 shares of common stock were outstanding as of June 30, 2020.
Financial Guidance

Cash position. As of June 30, 2020, we had cash, cash equivalents and investments of $249.8 million. Rocket expects such resources will be sufficient to fund its operations into the second quarter of 2022.

F-star Therapeutics to Participate in BTIG Virtual Biotechnology Conference

On August 5, 2020 F-star Therapeutics Ltd., a clinical-stage biopharmaceutical company focused on transforming the lives of patients with cancer through the development of innovative tetravalent bispecific (mAb2) antibodies, reported that Eliot Forster, Chief Executive Officer, will participate in a Fireside Chat at the BTIG Virtual Biotechnology Conference on Monday August 10, 2020 (Press release, F-star, AUG 5, 2020, View Source [SID1234562947]).

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Event: F-star Therapeutics Fireside Chat
Time: 1:00 – 1:25 PM ET | 6:00 – 6:25 PM BST
Webcast Link: F-star Therapeutics Fireside Chat

The Company will also be available for one to one meetings during the conference, on Monday August 10 and Tuesday August 11.

FDA Formally Accepts PharmaCyte Biotech’s Drug Master File for Company’s Pancreatic Cancer Therapy

On August 5, 2020 PharmaCyte Biotech, Inc. (OTCQB: PMCB), a biotechnology company focused on developing cellular therapies for cancer and diabetes using its signature live-cell encapsulation technology, Cell-in-a-Box, reportedthat the Drug Master File (DMF) that its partner, Austrianova, filed with the U.S. Food and Drug Administration (FDA) has been accepted without any questions or suggested changes (Press release, PharmaCyte Biotech, AUG 5, 2020, View Source [SID1234562946]).

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The FDA’s Center for Biologics Evaluation and Research (CBER) successfully processed PharmaCyte’s DMF, which provides all confidential and detailed information covering the production of the CypCaps final product that was produced by Austrianova and will be used in PharmaCyte’s planned clinical trial in locally advanced, inoperable pancreatic cancer (LAPC).

PharmaCyte’s Chief Executive Officer, Kenneth L. Waggoner, said, "CBER’s acceptance and processing of our Drug Master File without any questions or comments is a credit to the painstaking work and dedication by Austrianova and our consultants to ensuring that the entire process is properly conducted and completed before any further documents are submitted to the FDA.

"We now look forward to presenting the FDA with our Investigational New Drug Application very soon for our planned clinical trial in locally advanced, inoperable pancreatic cancer."

A DMF is submitted to the FDA to provide detailed information about facilities, processes and materials used in the manufacturing, processing and packaging of human drugs. It is a prerequisite to securing approval and commercialization and ensures confidentiality of proprietary information related to the Active Pharmaceutical Ingredient (API). The information contained in a DMF is used to support, among other things, an IND.

The DMF requirements are complex and specific, encompassing every detail involved with the manufacture of the API – from raw materials to analytical methods, process development and optimization. The scrutiny goes all the way back to the starting materials used in the API.

To learn more about PharmaCyte’s pancreatic cancer treatment and how it works inside the body to treat locally advanced inoperable pancreatic cancer, we encourage you to watch the company’s documentary video complete with medical animations at: View Source

Myovant Sciences Announces Further Financing Support from Sumitomo Dainippon Pharma and Commercial Collaboration with Sunovion Pharmaceuticals

On August 5, 2020 Myovant Sciences (NYSE: MYOV), a healthcare company focused on redefining care for women and for men, reported a USD 200 million low-interest, five-year term loan commitment from Sumitomo Dainippon Pharma Co., Ltd. (TSE: 4506), bringing its total financing support for Myovant to USD 600 million, further bolstering Myovant’s cash and committed funding and increasing the company’s financing flexibility as it prepares for multiple potential product launches to treat advanced prostate cancer, uterine fibroids, and endometriosis (Press release, Myovant Sciences, AUG 5, 2020, https://investors.myovant.com/news-releases/news-release-details/myovant-sciences-announces-further-financing-support-sumitomo [SID1234562945]).

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Additionally, Myovant announced that it has entered into a three-year commercial collaboration agreement with Sunovion Pharmaceuticals Inc. (Sunovion), an indirect, wholly-owned subsidiary of Sumitomo Dainippon Pharma, for services to support the planned commercialization of investigational drug candidate relugolix. Under the agreement, Sunovion will provide third-party logistics, trade and retail distribution, contract operations, and market access account management services to Myovant and will become a non-exclusive distributor of relugolix for prostate cancer and the exclusive distributor of relugolix combination tablet for uterine fibroids and endometriosis in the U.S.

"The financial and operational support we are receiving from Sumitomo Dainippon Pharma puts Myovant in a unique position with the potential to strengthen our launch readiness, enhance our financial performance, and maximize the opportunity for relugolix, as we head toward significant milestones for the company and stakeholders," said Frank Karbe, president and chief financial officer of Myovant Sciences. "We have made tremendous progress in building internal commercial capabilities across a number of areas and have forged important third-party relationships to leverage other well-established capabilities, as demonstrated by today’s agreement to access Sunovion’s successful and well-honed commercial infrastructure."

"We are pleased to enter into this commercial collaboration with Myovant," said Thomas Gibbs, senior vice president and chief commercial officer of Sunovion. "Our agreement enables access to Sunovion’s commercial and market access expertise to complement the commercial capabilities of Myovant, and we look forward to working closely with our partners at Myovant to prepare for the launch of relugolix."

The terms of the new loan facility are expected to be largely consistent with the initial USD 400 million low-interest, five-year term loan facility from Sumitomo Dainippon Pharma that was announced in December 2019, and does not provide Sumitomo Dainippon Pharma with any rights to relugolix. Myovant will be able to access the facility on a quarterly basis, subject to certain terms and conditions, with no repayments due until the end of the term subject to certain exceptions. The additional funds will be used to fund Myovant’s operating expenditures, including preparation for the commercialization of relugolix.

Relugolix (120 mg) is under Priority Review by the U.S. Food and Drug Administration (FDA) for the treatment of men with advanced prostate cancer, with a target action date of December 20, 2020. Additionally, Myovant submitted a Marketing Authorization Application to the European Medicines Agency in March 2020 and a New Drug Application to the FDA in May 2020 for relugolix combination tablet (relugolix 40 mg, estradiol 1.0 mg,