Innate Pharma Announces Conference Call and Webcast for Third Quarter 2022 Business Update

On November 7, 2022 Innate Pharma SA (Euronext Paris: IPH; Nasdaq: IPHA) ("Innate" or the "Company"), reported that the Company will hold a conference call on Monday, November 14, 2022, at 2 p.m. CET / 8 a.m. ET, to give an update on business progress during the third quarter of 2022 (Press release, Innate Pharma, NOV 7, 2022, View Source [SID1234623165]).

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Speakers during the call will be:

Mondher Mahjoubi, Chief Executive Officer
Joyson Karakunnel, Executive Vice President, Chief Medical Officer
Yannis Morel, Executive Vice President, Product Portfolio Strategy & Business Development
Frédéric Lombard, Senior Vice President, Chief Financial Officer
Details for the Virtual Event

The live webcast will be available at the following link:
View Source

Participants may also join via telephone to ask questions by registering in advance of the event at: View Source Upon registration, participants will be provided with dial-in numbers, a direct event passcode and a unique registrant ID that they may use 10 minutes prior to the event start to access the call. Call reminders will also be sent to registered participants via e-mail the day prior to the event.

This information can also be found on the Investors section of the Innate Pharma website, www.innate-pharma.com. A replay of the webcast will be available on the Company website for 90 days following the event.

Apros Therapeutics to Present Interim Clinical Data from a Phase 1 Study Evaluating APR003 at the 2022 Society for Immunotherapy of Cancer (SITC) Annual Meeting and World Vaccine & Immunotherapy Congress (WVIC) West Coast

On November 7, 2022 Apros Therapeutics reported that Interim Clinical Data from a Phase 1 Study Evaluating APR003 at the 2022 Society for Immunotherapy of Cancer (SITC) (Free SITC Whitepaper) Annual Meeting and World Vaccine & Immunotherapy Congress (WVIC) West Coast (Press release, Apros Therapeutics, NOV 7, 2022, View Source [SID1234623164])

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EISAI TO DIVEST RIGHTS FOR MUSCLE RELAXANT MYONAL® AND VERTIGO AND EQUILIBRIUM DISTURBANCE TREATMENT MERISLON® IN ASIA TO DKSH

On November 7, 2022 Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, "Eisai") reported that it has entered into an agreement to divest its rights for muscle relaxant Myonal (generic name: eperisone hydrochloride) and vertigo and equilibrium disturbance treatment Merislon (generic name: betahistine mesilate) in Asia (9 countries/regions*) to a subsidiary of DKSH Holding Ltd. (Headquarters: Zurich, Switzerland, "DKSH") (Press release, Eisai, NOV 7, 2022, View Source [SID1234623162]).

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In our Asia and Latin America Pharmaceuticals Business (ALA Region), we are shifting to a product portfolio centered on new global products in our strategic areas of neurology and oncology. Eisai believes that this divestiture agreement will accelerate the pursuit of the best marketing mix in the ALA Region. Under the terms of the agreement, Eisai will receive a contractual up-front payment, and also plan to supply the products. Eisai will retain its manufacturing rights to and continue to distribute the products in countries such as Japan, China and South Korea.

DKSH is a leading provider of "Market Expansion Services" that comprehensively supports companies’ business growth and entry into new markets, especially in Asia, and is already responsible for supplying Eisai’s products in some parts of Asia.

The agreement will enable Eisai to strategically reallocate resources to other mid-to-long-term business growth areas so as to continue to make further contributions to address the diversified needs of, and increase the benefits provided to, patients and their families.

*Cambodia, Indonesia, Laos, Malaysia, Myanmar, the Philippines (Myonal only), Singapore, Taiwan (Merislon only), Thailand

ImmunAdd attends Vaccines Summit 2022 in Washington DC

On November 6, 2022 ImmunAdd, a privately held pharmaceutical company developing a fully synthetic, rationally designed, saponin-based small molecule vaccine adjuvant, reported the company attended the Vaccines Summit 2022 in Washington DC on October 11-13 (Press release, ImmunAdd, NOV 6, 2022, View Source [SID1234654655]).

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Founder of ImmunAdd, Pi-Hui Liang, said "My team and I were delighted to attend the Vaccines Summit, an internationally renowned academic conference, where we presented a poster describing our state-of-the art vaccine adjuvant IA-05 and our business development team met with companies from all over the world."

The IA-05 vaccine adjuvant
IA-05 is a fully synthetic, rationally designed, saponin-based small molecule vaccine adjuvant which that has demonstrated improved tolerability and elicited improved enhanced immune responses compared with QS-21 in COVID, influenza, and anti-cancer vaccines. IA-05 can therefore enable the development of safer, more effective, and more durable vaccines and address the crisis faced by the South American soap bark tree (Quillaja Saponaria), which is being unsustainably harvested for QS-21 production. IA-05 is being tested in vaccines by several biopharmaceutical companies from different countries.

Telix Announces Positive Topline Results of ZIRCON Phase III Kidney Cancer Imaging Study

On November 6, 2022 Telix Pharmaceuticals Limited (ASX: TLX, Telix, the Company) reported highly positive top-line results from the pivotal Phase III ZIRCON study (Zirconium in Renal Cancer Oncology, NCT03849118) of its investigational renal (kidney) cancer positron emission tomography (PET) imaging agent, TLX250-CDx (89Zr-DFO-girentuximab) (Press release, Telix Pharmaceuticals, NOV 6, 2022, View Source [SID1234623168]). The study has met its co-primary and secondary endpoints.

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The study results delivered 86% sensitivity and 87% specificity, exceeding the pre-determined threshold required to demonstrate the ability of TLX250-CDx to reliably detect the clear cell phenotype and provide a non-invasive method of diagnosing the presence and spread of ccRCC. The study has also met the key secondary endpoint, achieving 85% sensitivity and 89% specificity in detecting ccRCC in tumours <4cm ("T1a" classification), currently a significant clinical challenge in the diagnosis of ccRCC.

A total of 300 patients were dosed with TLX250-CDx resulting in 284 evaluable patients. Each patient received a single dose of TLX250-CDx and a histological tumour sample from surgical resection was used as the truth comparator.

The results mean that, for the first time, urologists and urologic oncologists may have a non-invasive way to determine if small renal masses are the clear cell phenotype, the most aggressive and common form of renal malignancy. TLX250-CDx has received "Breakthrough Designation" from the FDA.1
Investigators in the ZIRCON study commented:2

A/Prof Brian Shuch, MD, Director, Kidney Cancer Program, UCLA Institute of Urologic Oncology (Los Angeles, California) said, "The positive result from the study is a critical step in better diagnosing clear cell renal cancer. Having an imaging product like TLX250-CDx will be so important in managing the continued increase in incidence of small renal masses and reducing the need for unnecessary invasive surgery for lesions that in the prior era were often found to be benign at the time of surgery."

Mr Gregory Jack, F.R.A.C.S., General Urological Surgeon Austin Health and Olivia Newton John Cancer Centre (Melbourne, Australia) added, "Kidney cancer is a diagnostic dilemma for the majority of our patients. Without biopsy or surgery, we can’t currently give them the information they need. Based on this result from the ZIRCON Phase III study, TLX250-CDx may help us to be more accurate in who we treat, whilst also providing reassurance for those patients who don’t need treatment."

Professor Françoise Kraeber-Bodéré, MD, PhD, Nuclear Medicine Department – CHU Nantes (Nantes, France), said, "Results from the Phase III ZIRCON study of TLX250-CDx should represent a major milestone in the management of small renal lesions and the diagnosis of clear cell renal cell carcinoma. There is so much potential in optimal targeting of CAIX, paving the way for better staging of this neoplasia and a theranostic approach."

Based on these outstanding results Telix intends to file a BLA for regulatory approval with the FDA and global regulatory agencies as a positron emission tomography/computed tomography (PET/CT) imaging agent for use in the characterisation of indeterminate renal masses previously identified on CT or MRI as ccRCC or non-ccRCC. Potential future utility may include active surveillance, surgical staging and treatment response assessment and the Company is actively engaged in clinical research at leading cancer centres to demonstrate the potential of these indications.

Dr Colin Hayward, Chief Medical Officer at Telix said: "The excellent sensitivity and specificity demonstrated in the ZIRCON study, validates that the CAIX target could be just as ground-breaking in ccRCC as PSMA3 and its application in PSMA-PET imaging has been for prostate cancer. It could optimise surgical intervention – particularly in the incidence of very small renal masses. These results provide confidence that TLX250-CDx is an important tool not only for initial diagnosis but potentially also for active surveillance and disease staging."