Celldex to Present at the Jefferies 2021 Virtual Healthcare Conference

On May 26, 2021 Celldex Therapeutics, Inc. (NASDAQ:CLDX) reported that senior management will participate in a fireside chat at the Jefferies 2021 Virtual Healthcare Conference on Wednesday, June 2, 2021 at 1:30 p.m. ET (Press release, Celldex Therapeutics, MAY 26, 2021, View Source [SID1234580698]).

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A webcast of the presentation will be available on the "Events & Presentations" page of the "Investors & Media" section of the Celldex website. A replay will be available for 30 days following the event.

Merus to Participate in a Fireside Chat at the Jefferies Virtual Healthcare Conference

On May 26, 2021 Merus N.V. (Nasdaq: MRUS), a clinical-stage oncology company developing innovative, full-length multispecific antibodies (Biclonics and Triclonics), reported that Bill Lundberg, M.D., Chief Executive Officer of Merus, will participate in a fireside chat at the Jefferies Virtual Healthcare Conference on Wednesday, June 2 at 9:00 a.m. ET (Press release, Merus, MAY 26, 2021, View Source [SID1234580697]).

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The live webcast of the presentation will be available on the Investors page of the Company’s website. An archived presentation will be available on the Merus website for a limited time.

IMMUTEP GRANTED CHINESE PATENT FOR EFTILAGIMOD ALPHA IN CHEMO-IMMUNOTHERAPY COMBINATION

On May 26, 2021 Immutep Limited (ASX: IMM; NASDAQ: IMMP) ("Immutep" or "the Company"), a biotechnology company developing novel immunotherapy treatments for cancer and autoimmune disease, reported the grant of a new patent (number ZL201480073584.3) entitled "Combined Preparations for the Treatment of Cancer" by the Chinese Patent Office (Press release, Immutep, MAY 26, 2021, View Source [SID1234580677]).

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This Chinese patent follows the grant of the corresponding European, Australian, Japanese and United States patents, as announced separately throughout 2019 and 2020. The new patent protects Immutep’s intellectual property relating to combination therapy comprising (a) lead active immunotherapy candidate eftilagimod alpha (efti or IMP321), which is a LAG-3 fusion protein (LAG-3Ig), and (b) a chemotherapy agent. The chemotherapy agent is oxaliplatin, carboplatin, or topotecan, and the patent provides protection in the territory of mainland China.

The new patent is owned by Immutep S.A.S. and exclusively licensed to Immutep’s partner in China, EOC Pharma ("EOC"). The patent expiry date is 19 December 2034.

Dr. Frédéric Triebel, Immutep’s Chief Scientific Officer and Chief Medical Officer, noted: "Oxaliplatin, carboplatin and topotecan continue to be commonly used forms of chemotherapy in China and more broadly. Furthermore, combinations of chemotherapy and active immunotherapies have begun to be approved for the treatment of advanced solid tumors in recent years. As such, this new patent provides protection in the important Chinese territory for a range of novel and highly relevant chemo-immunotherapies featuring efti that could be developed in the future by our partner, EOC Pharma."

EOC Pharma CEO, Xiaoming Zou, said: "We are very pleased that our partner, Immutep, continues to make important progress in building a robust patent estate around efti. This underpins our continued investment in this unique and promising candidate, and provides a range of future development options for our business."

About efti in China

Efti is exclusively licensed to EOC for the territory of Greater China (namely mainland China, Hong Kong S.A.R, Macao S.A.R. and Taiwan). Under its agreement with Immutep, EOC will make further milestone payments to the Company if efti achieves specific development milestones, as well as pay sales-based royalties.

ORIC Pharmaceuticals to Present at Jefferies Virtual Healthcare Conference

On May 26, 2021 ORIC Pharmaceuticals, Inc. (Nasdaq: ORIC), a clinical stage oncology company focused on developing treatments that address mechanisms of therapeutic resistance, reported that Jacob Chacko, M.D., chief executive officer, will participate in a fireside chat at the Jefferies Virtual Healthcare Conference on Friday, June 4, 2021, at 1:30 p.m. ET (Press release, ORIC Pharmaceuticals, MAY 26, 2021, View Source [SID1234580663]).

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A live webcast of the fireside chat will be available through the investor section of the company’s website at www.oricpharma.com. A replay of the webcast will be available for 90 days following the event.

Nordic Nanovector ASA: Results for the First Quarter 2021

On May 26, 2021 Nordic Nanovector ASA (OSE: NANOV) reported its results for the first quarter 2021 (Press release, Nordic Nanovector, MAY 26, 2021, View Source [SID1234580658]). A live webcast presentation by Nordic Nanovector’s management team will take place today at 08.30 CEST. A link to the webcast is available on www.nordicnanovector.com.

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The results report and the presentation are also available on the company’s website in the section: Investors & Media/Reports and Presentation/Interim Reports/2021. A replay of the webcast will be made available at the same location after the event.

Peter L. Braun, Chief Executive Officer of Nordic Nanovector, commented: "Nordic Nanovector has made important progress so far in 2021, including raising the money needed to deliver the preliminary top-line three-month data from the PARADIGME study and to prepare for a subsequent potential BLA filing for Betalutin. The company has also implemented a range of initiatives aimed at improving patient recruitment into PARADIGME, and which we believe will further improve patient enrolment when the impact of COVID-19 recedes. I am convinced that effective and well-tolerated, targeted radiopharmaceuticals, such as Betalutin, a one-time treatment, can make a real difference to NHL patients worldwide."

Operational Highlights

Peter L. Braun was appointed Chief Executive Officer in March
Mr Braun is an experienced and entrepreneurial pharmaceutical leader with extensive commercialisation and innovative oncology experience from a career spanning nearly 30 years at Roche
Successful Private Placement and oversubscribed Repair Offering completed in February and April, respectively, raised approximately NOK 422 million (USD 49.7 million) in gross proceeds
Extends the company’s cash runway into H2’2022
Operational improvements and protocol changes have improved PARADIGME recruitment rate in recent months, despite impact from the on-going COVID-19 pandemic
83 patients enrolled as of 25 May 2021 (73 enrolled as of 17 February 2020)
Company remains on track to report preliminary three-month top-line data by the end of 2021
Promising Phase 1b data from the Archer-1 study evaluating Betalutin in combination with rituximab in 2L FL
Board changes
Hilde Hermansen Steineger, PhD, decided not to stand for re-election at AGM
Solveig Hellebust, PhD, appointed Non-executive Director at the AGM on 28 April 2021
Financial Highlights Q1 2021

(Figures in brackets = same period 2020 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 101.2 million (NOK 125.9 million).
Research and development (preclinical, clinical, medical affairs, regulatory and CMC activities) expenses accounted for 85.9 % of total operating expenses year to date 2021 (80.8 %).
Comprehensive loss for the first quarter amounted to NOK 102.1 million (loss of NOK 91.7 million).
Cash and cash equivalents at the end of March 2021 amounted to NOK 497.9 million, compared to NOK 294.0 million at the end of December 2020.
Outlook

Nordic Nanovector’s current focus is to complete patient enrolment into PARADIGME and the target is to announce the preliminary readout of three-month top line data from PARADIGME by end 2021.

Following the recent successful Private Placement and Repair Offering, the company has extended its cash runway into H2’2022, which in addition to allowing it to deliver the top line data from PARADIGME, will enable further preparatory work on the potential Betalutin BLA filing to be undertaken.

The company believes that, if positive, the PARADIGME trial data could represent a significant value inflection point for the company and its shareholders, confirming Betalutin as a highly promising new targeted radioimmunotherapy that can address the unmet needs of R/R FL patients.