Incyte to Present at Upcoming Investor Conference

On September 1, 2020 Incyte (Nasdaq:INCY) reported that it will present at the Morgan Stanley 18th Annual Global Healthcare (Virtual) Conference on Wednesday, September 16, 2020 at 9:30 a.m. EDT (Press release, Incyte, SEP 1, 2020, View Source [SID1234564218]).

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The presentation will be webcast live and can be accessed at Investor.Incyte.com and will be available for replay for 30 days.

Invitae to Participate in the Morgan Stanley Virtual Global Healthcare Conference

On September 1, 2020 Invitae Corporation (NYSE: NVTA), a leading medical genetics company, reported that members of its management team will virtually participate in a fireside chat at the 18th Annual Morgan Stanley Global Healthcare Conference on Monday, September 14, 2020 at 4:30 p.m. Eastern / 1:30 p.m. Pacific (Press release, Invitae, SEP 1, 2020, View Source [SID1234564217]).

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Invitae’s (NVTA) mission is to bring comprehensive genetic information into mainstream medical practice to improve the quality of healthcare for billions of people. www.invitae.com (PRNewsFoto/Invitae Corporation)

The live webcast of the fireside chat may be accessed by visiting the investors section of the company’s website at ir.invitae.com. A replay of the webcast will be available shortly after the conclusion of the fireside chat.

Invitation to presentation of Oasmia’s Q1 report 2020/2021 on September 9, 2020

On September 1, 2020 Oasmia Pharmaceutical reported that it will publish its Q1 report on September 9, 2020, at 08.00 am CEST (Press release, Oasmia, SEP 1, 2020, View Source [SID1234564215]).

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The company will hold a conference call and an online presentation on the same day at 10.00 am CET. The call will be hosted by Francois Martelet, CEO, and Michael af Winklerfelt, CFO. The presentation will be in English.

DCprime and PCI Biotech Announce a Research Collaboration to Explore Novel Cancer Vaccination Concepts

On September 1, 2020 DCprime, the front-runner in the field of relapse vaccines, and PCI Biotech (OSE: PCIB), a cancer focused biopharmaceutical company with a unique intracellular delivery technology via PhotoChemical Internalisation, reported an extensive research collaboration (Press release, DCPrime, SEP 1, 2020, View Source [SID1234564214]). Within the collaboration, DCprime and PCI Biotech will combine their know-how and technology platforms to pursue the development of novel cancer vaccination concepts based on tumor-independent antigens (TIAs). The collaboration builds on preclinical proof-of-concept results previously presented by DCprime at the 34th Annual Meeting of the Society for Immunotherapy of Cancer (SITC) (Free SITC Whitepaper) in November 2019 and on PCI Biotech fimaVacc and fimaNAc technologies.

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The partnership is governed by a research collaboration agreement, under which the collaborators will perform an extensive evaluation of technology compatibility and synergy based on preclinical studies. The companies will evaluate results achieved from this research collaboration and then explore the potential for further development and partnership.

"We continue to innovate the cancer vaccine space and look forward to working closely with PCI Biotech on a ground-breaking off-the shelf vaccination concept for solid tumors addressing the huge need for novel antigen targets in oncology," said Erik Manting, CEO of DCprime. " Having access to PCI Biotech’s intracellular antigen delivery platforms and expertise will accelerate the development of therapeutic approaches based on the unique and novel principle we developed using tumor-independent antigens. This complements DCprime’s existing pipeline of relapse vaccines progressing through clinical trials in haematological malignancies."

"We are very pleased to collaborate with DCprime. This collaboration could reinforce the fimaVacc positive results obtained during a phase I study presented at the European Society for Medical Oncology (ESMO) (Free ESMO Whitepaper) Immuno-Oncology Congress 2019, and the preclinical promising results obtained with fimaNAc, the PCI-mediated intracellular delivery of various types of "naked" mRNA molecules. Combining the complementary technologies of DCprime and PCI Biotech could lead to entirely new therapeutic clinical applications," commented Per Walday, CEO of PCI Biotech.

Strengthened patent protection for arfolitixorin in Japan

On September 1, 2020 Isofol Medical AB (publ), (Nasdaq First North Premier Growth Market: ISOFOL), reported that the company has further strengthened its position in the second largest market for treatment of mCRC by obtaining two new patent grants for arfolitixorin in Japan (Press release, Isofol Medical, SEP 1, 2020, View Source [SID1234564213]). One relates to the preparation process of the drug for injection and one relates to the dosage regimens, including those applied in the ongoing global Phase III study AGENT. Together with the already granted Active Substance Patent (API), these two patents will ensure a strong and extended patent protection for the important future Japanese market until 2038.

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One patent covers the processes to prepare the clinical product for injection and is a divisional patent application (JP 2018-164332) of an earlier approved patent (JP 6617104). The now approved divisional patent is considered very important for Isofol because it, more explicitly, provides protection for preparing the Lyophilisate (freeze dried) Clinical Product, from the API (arfolitixorin hemisulfate). This patent is valid until 2034.

The other newly granted patent is a use patent (JP 6734308) with dose regimens including "multiple bolus injections" of arfolitixorin as an important feature in combination with both bolus injection and infusion of the anti-cancer agent 5-FU. This patent covers the ongoing AGENT study regimen with respect to dose levels and timings. This patent is valid until 2038.

Ulf Jungnelius, CEO of Isofol, commented: "It is most gratifying that we now have strengthened our patent rights in the Japanese market as well. Combined with our recently concluded license agreement with Solasia Pharma K.K. in Japan, we have a promising position for commercial opportunities in the second largest global market for the treatment of mCRC."

The information was submitted for publication, through the agency of the contact person set out above, at 09:00 PM CEST on September 1, 2020.

About arfolitixorin
Arfolitixorin is Isofol’s proprietary drug candidate being developed to increase the efficacy of standard of care chemotherapy for advanced colorectal cancer. The drug candidate is currently being studied in a global Phase 3 study, AGENT. As the key active metabolite of the widely used folate-based drugs, arfolitixorin can potentially benefit all patients with advanced colorectal cancer, as it does not require complicated metabolic activation to become effective.