Cellectis and Lonza Enter cGMP Manufacturing Service Agreement for Cellectis’ Allogeneic UCART Product Candidates

On October 1, 2019 Cellectis (Euronext Growth: ALCLS – Nasdaq: CLLS), a clinical-stage biopharmaceutical company focused on developing immunotherapies based on allogeneic gene-edited CAR T-cells (UCART), and Lonza (SWX: LONN), reported that the companies have entered into a manufacturing service agreement covering clinical manufacturing of Cellectis’ allogeneic UCART product candidates targeting hematological malignancies (Press release, Cellectis, OCT 1, 2019, View Source [SID1234550314]). Lonza is in charge of implementing Cellectis’ manufacturing processes as per current Good Manufacturing Practices (cGMP) in a way that meets the highest quality and safety standards outlined by the FDA. The manufacturing will take place at Lonza’s GMP facility in Geleen, Netherlands.

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

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

                  Schedule Your 30 min Free Demo!

William Monteith, Executive Vice President, Technical Operations, Cellectis:
"Working with Lonza, a world-class solutions provider with deep experience in the biotech and pharma industries increases our global capabilities and allows Cellectis to further strengthen its manufacturing expertise. This agreement not only bolsters our product supply for clinical trials, but it ensures that we are producing first-rate product candidates so that we can potentially deliver new hope to patients living with certain blood cancers."

Alberto Santagostino, Senior Vice President, Head of Cell & Gene Technologies, Lonza:
"Early-stage innovators with great science, like Cellectis, can find an ideal partner in Lonza as we bring great value in technical development and manufacturing, industrializing processes and enabling the journey to commercialization. We will draw on the experience at our cell and gene therapy center of excellence in the Netherlands, ideally equipped to support Cellectis in bringing their promising pipeline of allogeneic CAR-T therapies to people around the world in need of life-saving products."

Lonza’s supply will complement Cellectis’ ongoing collaboration and in-house manufacturing sites, IMPACT and SMART, which are currently under construction.

The manufacturing process of Cellectis’ allogeneic CAR T-cell product line, Universal CARTs or UCARTs, yields frozen, off-the-shelf, non-alloreactive engineered CAR T-cells. UCARTs are intended to be readily available CAR T-cells for a large patient population. Their production is industrialized with defined pharmaceutical release criteria.

Ryvu Therapeutics and Selvita Announce Registration of Corporate Split by the National Court Register of Poland

On October 1, 2019 Ryvu Therapeutics and Selvita (WSE: SLV) reported that the National Court Register of Poland ("KRS") has recognized the corporate split of the Selvita parent company into two distinct organizations (Press release, Ryvu Therapeutics, OCT 1, 2019, View Source [SID1234542463]). The recognition by the court follows the Sept. 19, 2019, shareholder resolution to separate oncology therapeutics and contract research (CRO) business units.

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

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

                  Schedule Your 30 min Free Demo!

Going forward, Ryvu Therapeutics and Selvita (CRO) will now operate independently with separate executive management teams as well as supervisory boards, in accordance with the shareholder resolution.

Public trading of Ryvu Therapeutics under the symbol RVU, separated from Selvita is expected to begin on or about 9th October, subject to approvals from the National Depository for Securities ("KDPW") and the Warsaw Stock Exchange ("GPW").

Until this time, the value of the two independent companies will be reflected under the current listing of Selvita on the Warsaw Stock exchange.

Public listing of the contract research organization Selvita (CRO) under the symbol SLV is also expected on or about 16th October.

Stealth Biotherapeutics to Present at the 2019 Cantor Global Healthcare Conference

On October 1, 2019 Stealth BioTherapeutics Corp (NASDAQ: MITO), a clinical-stage biotechnology company focused on the discovery, development and commercialization of novel therapies for diseases involving mitochondrial dysfunction, reported that Reenie McCarthy, Chief Executive Officer, will present at the 2019 Cantor Global Healthcare Conference on Wednesday, October 2, 2019 at 5:20 p.m. ET in New York (Press release, Stealth Biologics, OCT 1, 2019, View Source [SID1234540002]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

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

                  Schedule Your 30 min Free Demo!

A live audio webcast of the presentation will be available on the Investors & News section of Stealth’s website at https://investor.stealthbt.com/. A replay of the webcast will be archived on Stealth’s website for 30 days following the event.

Immunicom Secures an Additional $1.85 Million Bringing its Series B Funding to $12.85 Million

On October 1, 2019 Immunicom, Inc., a medical technology company reported that has been awarded FDA Breakthrough Device Designation for its non-pharmaceutical solution for treating stage IV metastatic cancer, gained an additional $1.85 million towards its Series B investment round on September 9th (Press release, Immunicom, OCT 1, 2019, View Source [SID1234540001]). This increases Immunicom’s overall capital raised to $21.85 million.

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

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

                  Schedule Your 30 min Free Demo!

Immunicom has also hired Raju Chauhan as Vice President of Program Management to provide guidance and oversight to both internal and customer facing initiatives. "We are very fortunate to add Raju to Immunicom’s growing team," said Amir Jafri, the company’s Founder and CEO. "With Raju on our team we will be more proficient in achieving our fast-paced global business deals and groundbreaking research goals to accelerate bringing Immunopheresis to the world."

Raju has over 30 years of experience working in the technology development and managing teams across the globe with a proven record of creating and delivering, innovative, cost-effective solutions for mission-critical business problems. He has been an integral part of managing projects for several fortune 50 companies as well as healthcare space. At Cardinal Health, Raju managed teams spread across several locations in USA. Raju has also managed and worked with many different teams in several countries including Canada, China, India, and Ukraine. Raju has worked in many different industries including Medical Device Manufacturers, Healthcare, Oil and Gas, Software, Telecommunications, Food and Beverages, Airlines, Credit Bureaus, Background Checks, Real Estate, Professional Services and Utilities.

Raju received his Master of Computer Science degree from Mississippi State University.

AIVITA Biomedical to Present at Meeting on the Mesa and Other Investor, Oncology and Regenerative Medicine Conferences in October

On October 1, 2019 AIVITA Biomedical, Inc., a biotech company specializing in innovative stem cell applications, reported that it will be presenting at the following investor, oncology and regenerative medicine conferences in October (Press release, AIVITA Biomedical, OCT 1, 2019, View Source [SID1234540000]):

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

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

                  Schedule Your 30 min Free Demo!

Cell & Gene Meeting on the Mesa
Company Presentation
Time: October 2, 11:00 AM PST
Location: Park Hyatt Aviara Resort Golf Club & Spa, Cognate in the Bioservices Ballroom, Carlsbad, CA

World Immunotherapy Congress
Keynote Title: Enhancing patient responses with autologous cancer stem cell vaccine in combination with checkpoint inhibitors
Time: October 16, 9:25 AM CET
Location: Congress Centre Basel, Basel, Switzerland

BIO Investor Forum
Company Presentation
Time: October 23, 10:15 AM PST
Location: Elizabethan A, The Westin St. Francis, San Francisco, CA

World Vaccine Congress
Talk Title: Autologous Cancer Stem Cell Vaccines for Solid Tumor Cancers
When: October 29, 3:45 PM CET
Location: Palau de Congressos de Catalunya, Barcelona, Spain