NKGen Biotech to Present at the Baird 2022 Global Healthcare Conference

On September 7, 2022 NKGen Biotech, a biotechnology company harnessing the power of the body’s immune system through the development of Natural Killer (NK) cell therapies, reported that its senior management will present at the Baird 2022 Global Healthcare Conference on Wednesday, September 14, 2022, in New York City (Press release, NKMax America, SEP 7, 2022, View Source [SID1234619145]). Please see details below:

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NKGen Biotech will also hold one-on-one investor meetings. To schedule a meeting, please contact your Baird representative.

Exercise of Options

On September 7, 2022 ImmuPharma plc (LSE : IMM), the specialist drug discovery and development company, reported that L1 Capital Global Opportunities Master Fund ("L1") has exercised Options over 3,000,000 new ordinary shares of 1p each ("Ordinary Shares") at an exercise price of 5p per share, for a consideration of £150,000 (Press release, ImmuPharma, SEP 7, 2022, View Source [SID1234619144]).

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New Ordinary Shares and Admission

The New Ordinary Shares have been allotted today and are issued credited as fully paid and will rank pari passu in all respects with the Company’s existing issued ordinary shares.

An application will be made for the New Ordinary Shares to be admitted to trading on the AIM market ("Admission") of the London Stock Exchange. It is anticipated that Admission will occur on or around Tuesday 13 September 2022.

The New Ordinary Shares represent 0.90% of the Company’s enlarged issued share capital.

Total Shares in Issue

For the purposes of the Disclosure Guidance and Transparency Rules of the Financial Conduct Authority ("DTR"), the Board of ImmuPharma hereby notifies the market that following Admission, the Company’s total issued share capital will consist of 333,403,115 Ordinary Shares with a nominal value of 1p each.

This figure may be used by Shareholders as the denominator for the calculations by which they may determine if they are required to notify their interest in, or a change to their interest in, the Company under the DTR.

This announcement contains inside information for the purposes of Article 7 of EU Regulation 596/2014.

ImmixBio Completes GMP Manufacturing of Scaled-Up Batch of IMX-110 for Clinical Trials

On September 7, 2022 Immix Biopharma, Inc. (Nasdaq: IMMX) ("ImmixBio", "Company", "We" or "Us"), a biopharmaceutical company pioneering Tissue-Specific Therapeutics (TSTx) targeting oncology and immuno-dysregulated diseases, reported that it has completed Good Manufacturing Practice ("GMP") manufacturing of a scaled-up batch of IMX-110 for clinical trials. IMX-110 was produced using our proprietary, scaled-up manufacturing process that will provide drug supply for 2 ImmixBio clinical trials planned to start in 2022: first, planned monotherapy IMX-110 clinical trial in soft tissue sarcoma ("STS"); second, planned combination IMX-110 + BeiGene anti-PD-1 tislelizumab clinical trial in advanced solid tumors (Press release, Immix Biopharma, SEP 7, 2022, View Source [SID1234619143]).

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"Completing the first batch of GMP IMX-110 using our proprietary, scaled-up GMP manufacturing process just 7 months after our manufacturing kick-off is a testament to the efficiency and dedication of our stellar team," said Ilya Rachman, MD PhD, CEO of ImmixBio. "Building on promising clinical and animal data for IMX-110 as a monotherapy and in combination with PD-1, we are excited to kick off 2 clinical trials soon in 2022 – IMX-110 monotherapy, and IMX-110 combined with BeiGene anti-PD-1 tislelizumab."

About IMX-110

The U.S. Food and Drug Administration ("FDA") has approved orphan drug designation ("ODD") for IMX-110 for the treatment of soft tissue sarcoma. Additionally, the FDA has approved rare pediatric disease designation ("RPDD") for IMX-110 for the treatment of a life-threatening pediatric cancer in children, rhabdomyosarcoma. RPDD qualifies ImmixBio to receive fast track review and a priority review voucher (PRV) at the time of marketing approval of IMX-110. IMX-110 is currently being evaluated in a phase 1b/2a clinical trial in patients with advanced solid tumors. Learn more at www.immixbio.com/iMX-110.

CorMedix Inc. to present at the H.C. Wainwright Annual Global investment conference

On September 7, 2022 CorMedix Inc. (Nasdaq: CRMD), a biopharmaceutical company focused on developing and commercializing therapeutic products for the prevention and treatment of infectious and inflammatory disease, reported that management will be presenting a corporate overview at the H.C. Wainwright Annual Global Investment Conference being held in New Yok on September 12 – 14, 2022 (Press release, CorMedix, SEP 7, 2022, https://www.cormedix.com/cormedix-inc-to-present-at-the-h-c-wainwright-annual-global-investment-conference/ [SID1234619142]).

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Monteris Medical Announces First Patient Enrolled in REMASTer Clinical Study on NeuroBlate® System for Metastatic Brain Tumor Patients

On September 7, 2022 Monteris Medical reported that the first patient has been enrolled in its REMASTer (Recurrent Brain Metastases After Stereotactic Radiosurgery [SRS] Trial) clinical trial (Press release, Monteris Medical, SEP 7, 2022, View Source [SID1234619141]). This randomized controlled study is designed to investigate laser interstitial thermal therapy (LITT) using the NeuroBlate System as an early intervention for radiographically progressive brain metastases and to provide Level I evidence to guide treatment for this complex patient population.

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Treatment of recurrent brain metastases is challenging as no standardized care currently exists within the clinical community for patients with disease progression following SRS. This is primarily attributed to the uncertainty of the underlying cause being either recurrence or radiation necrosis. In recent years, LITT has proved to be an effective tool for both causes of progression after SRS and can be performed during the same procedure as needle biopsy. Recent published studies suggest that LITT plus SRS may be superior to LITT alone or repeat SRS alone for treatment of biopsy-proven brain metastasis recurrence after SRS failure, even after controlling for variables known to predict progression. Recent literature also has revealed LITT to be effective for the treatment of radiation necrosis, with a superior time to steroid independence compared to medical management alone.

The REMASTer trial is designed to determine the superior treatment algorithm for both the recurrent tumor and radiation necrosis populations. The study will enroll 154 patients at up to 12 sites. Primary endpoints for the study include time to local intracranial progression or death and time to steroid cessation. Additional endpoints include comparison of treatment approaches with respect to overall survival, quality of life, and cognitive changes over time.

"The REMASTer trial will be vital in providing Level I evidence that establishes a critically needed standard of care in patients who have radiographically progressive metastatic disease, be it radiation necrosis or true disease recurrence," said Dr. Peter Fecci, director of the Brain Tumor Immunotherapy Program and the Center for Brain and Spine Metastasis at Duke University School of Medicine in Durham, N.C. and REMASTer principal investigator. "Rapidly establishing steroid independence in the radiation necrosis population in the era of immunotherapy is crucial, as is optimizing freedom from local progression in patients with truly recurrent brain metastatic disease. This study will help to solidify the role for LITT in both scenarios."

It is estimated that up to 300,000 patients in the United States are diagnosed annually with metastatic brain tumors. The incidence of metastatic brain tumors has risen in recent years due to patients living longer with systemic cancers as a result of treatment advances, increased imaging procedures and early detection, and improvements in imaging technology. Metastatic tumor progression and radiation necrosis are therefore increasing in prevalence as well, necessitating the need for standard of care approaches to patient treatment.

"While the data supporting the use of LITT in radiation necrosis and recurrent metastatic disease is already strong enough to warrant inclusion in National Comprehensive Cancer Network guidelines, evidence is lacking to advise the best time for LITT in the treatment algorithm for patients with radiographic progression," said Jennifer Englund, vice president of clinical and regulatory affairs of Monteris. "We believe the study Dr. Fecci has designed is poised to deliver meaningful results that will standardize treatment for this growing population of patients."