NH TherAguix announces the enrolment in Boston of the first 2 patients in its clinical trials NANOBRAINMETS and NANOSMART

On October 1, 2021 NH TherAguix ("NHT"), a French clinical stage company specialising in the development of innovative nano medicines for the radiotherapy treatment of cancer indications, reported the enrolment of the 2 first patients in the NANOBRAINMETS Phase II trial targeting brain metastases and the NANOSMART Phase I/II trial targeting pancreatic cancer and cancerous lung lesions, sponsored by Dana-Farber Brigham Cancer Center and led by radiation oncologists Drs. Ayal Aizer and Jonathan E. Leeman, respectively (Press release, NH TherAguix, OCT 1, 2021, View Source;utm_medium=rss&utm_campaign=nh-theraguix-announces-the-enrolment-in-boston-of-the-first-2-patients-in-its-clinical-trials-nanobrainmets-and-nanosmart [SID1234590625]).

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These 2 randomized clinical trials will investigate the efficacy of the combination of AGuIX(R) intravenous injection with standard of care radiotherapy to increase survival and quality of life of patients.

NANOBRAINMETS is a double-blind, placebo-controlled randomized Phase II clinical trial of stereotactic radiation with or without AGuIX(R) gadolinium-based nanoparticles in the management of brain metastases at higher-risk of local recurrence with radiation alone. The objective is to test the hypothesis that, among 134 patients with brain metastases at higher-risk of local recurrence with radiation alone, AGuIX(R) gadolinium-based nanoparticles combined with brain-directed stereotactic radiation will improve local control, using Response Assessment in Neuro-Oncology – Brain Metastasis (RANO-BM) criteria, relative to brain-directed stereotactic radiation alone. This study follows the results already obtained by NH TherAguix through the NANORAD Phase I trial that demonstrated very promising results[1].

Dr. Ayal Aizer stated, "Increasingly, the mainstay of management for patients with brain metastases involves brain-directed stereotactic radiation. However, prior studies have identified subsets of patients with brain metastases for whom such radiation may be insufficient to achieve an efficient treatment. We have been searching for methods to safely and viably enhance radiation effect in these patients. Our study will provide insight as to whether AGuIX(R) is of potential benefit to patients with difficult to control brain metastases. We are enthusiastic about offering this study to patients managed at Dana-Farber Brigham Cancer Center."

NANOSMART is a Phase Ib/II clinical trial, with two treatment arms for patients diagnosed with either locally advanced pancreatic cancer or centrally located cancerous lung lesions. The radiotherapy will be performed using an MRI-Linac machine, allowing for the delivery of precise MRI-guided radiotherapy after intravenous AGuIX(R) injection.

During the Phase Ib part of the trial, patients will receive five fractions of stereotactic body radiation therapy in addition to one dose of AGuIX(R) nanoparticles seven days prior to radiation treatment and another one with the first fraction of radiation. Patients with cancerous lung lesions receiving radiation over a two-week period will be provided with an additional dose of AGuIX(R) along the fourth fraction of radiation. The Phase Ib part of the study will establish the dose of the drug used for each disease cohort during Phase II. At this point patients will be randomized to receive AGuIX(R) or not. NH TherAguix and Dana-Farber Brigham Cancer Center target an enrolment of 100 patients.

Dr. Jonathan E. Leeman stated, "There is a critical need to improve outcomes for patients with locally advanced unresectable pancreatic cancer or with centrally located lung tumors where effective treatments are limited. We believe this to be a very important study, which will evaluate the safety and benefits of AGuIX(R) gadolinium-based nanoparticles in combination with highly precise radiotherapy delivered using our MRI linear accelerator at the Dana-Farber Brigham Cancer Center. We greatly look forward to offering this opportunity to our patients."

"The launching of these 2 clinical trials the with Dana-Farber Brigham Cancer Center as the sponsor in the United States is a very important and significant step in our clinical development. This trial with Dana-Farber Brigham Cancer Center echoes with a historical and visionary collaboration initiated and pursued by Prof. Olivier Tillement and Dr. François Lux, co-founders of NH TherAguix (ILM, University of Lyon, France), and Dr. Ross Berbeco (Director of Medical Physics Research, Dana-Farber Brigham Cancer Center). Their drive for developing nanomedicine using AGuIX(R) started in 2010 and resulted in significant patents and scientific publications. This collaboration is still very active through an NIH grant of nearly $3M awarded to NH TherAguix in 2020 for the AGuIX(R) second generation platform. We are very grateful and happy about this long-term relationship with our US colleagues," said Géraldine Le Duc as CEO of NH TherAguix.

Following the enrolment of the 2 first patients in its clinical trials NANOBRAINMETS and NANOSMART, the clinical trials pipeline of NH TherAguix is as follows, with 4 clinical trials currently recruiting and 3 more expecting to be launched by the end of 2021:

About AGuIX(R):

AGuIX(R) is a bimodal nanomedicine, with a radiosensitizing effect and visible in MRI that has been extensively published (>70 papers). AGuIX(R) demonstrated a good post-injection safety, MRI contrast enhancement and early evidence of radiosensitization when combined with radiation therapy in patients with brain metastases (NANORAD 1 Phase Ib trial, Grenoble Alpes University Hospital, France). AGuIX(R) is currently also being tested through another Phase II trial in brain metastasis, using whole brain radiation therapy (NANORAD 2). In parallel, a Phase Ib trial for advanced cancer of the cervix (NANOCOL) is underway at the Gustave Roussy Institute in Paris.

Potential Response Predictors to IMV’s Lead Compound in the DeCidE Clinical Study in Patients with Advanced, Recurrent Ovarian Cancer to be Presented at SITC Annual Meeting

On October 1, 2021 IMV Inc. (NASDAQ: IMV; TSX: IMV), a clinical-stage biopharmaceutical company pioneering a novel class of immunotherapies against difficult-to-treat cancers, reported that a poster describing translational data obtained in the DeCidE clinical study in patients with advanced, recurrent ovarian cancer will be presented at the upcoming Society for Immunotherapy of Cancer (SITC) (Free SITC Whitepaper) Annual Meeting on November 10-14, 2021 in Washington, DC (Press release, IMV, OCT 1, 2021, sec.gov/Archives/edgar/data/1734768/000117625621000258/exhibit99-1.htm [SID1234590623]).

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Poster Title: Identification of potential response predictors to maveropepimut-S (DPX-Survivac), a novel T cell activating immunotherapy, in patients with advanced recurrent ovarian cancer

Presenter:

Oliver Dorigo, M.D., Ph.D.,
Director and Associate Professor
Division Gynecologic Oncology
Department of Obstetrics and Gynecology
Stanford University, CA
Poster Number: 353

Important dates

November 9, 2021: Full abstracts are made public at 8 a.m. EST

November 12, 2021: Poster presentation

Poster Hall Hours: 7 a.m.–8:30 p.m.

Dr. Dorigo will be present in person at lunch time (12:40–2:10 p.m. EST) and during the poster reception (7–8:30 p.m. EST)

November 12, 2021: Poster and e-poster presentation will be available under the Scientific Publications & Posters section on IMV’s website.

Nkarta to Present Preclinical Data from Engineered NK Cell Platform at SITC 36th Annual Meeting

On October 1, 2021 Nkarta, Inc. (Nasdaq: NKTX), a biopharmaceutical company developing engineered natural killer (NK) cell therapies to treat cancer, reported four presentations at the upcoming Society for Immunotherapy of Cancer (SITC) (Free SITC Whitepaper) 36TH Annual Meeting and Pre-Conference Programs to be held November 10-14, 2021 (Press release, Nkarta, OCT 1, 2021, View Source [SID1234590616]).

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The full abstracts are scheduled to be available on the SITC (Free SITC Whitepaper) website on November 9, 2021.

Presented jointly with CRISPR Therapeutics:

Title:
A Combined Strategy of CD70 CAR Co-expression with Membrane-bound IL-15 and CISH Knockout Results in Enhanced NK Cytotoxicity and Persistence
Abstract Number and Type:
16439, oral*
Poster Presentation Date and Time:
November 10, 2021, 2:40 p.m. ET

Title:
CISH Gene-knockout Anti-CD70-CAR NK Cells Demonstrate Potent Anti-tumor Activity Against Solid Tumor Cell Lines and Provide Partial Resistance to Tumor Microenvironment Inhibition
Abstract Number and Type:
113, poster
Poster Presentation Date and Time:
November 12, 2021, 7:00 am – 8:30 pm ET

Nkarta presentations:

Title:
Potentiating the Large-Scale Expansion and Engineering of Peripheral Blood-Derived CAR NK Cells for Off-the-Shelf Application
Abstract Number and Type:
151, poster
Poster Presentation Date and Time:
November 12, 2021, 7:00 am – 8:30 pm ET

Title:
KIR Haplotype Can Inform Donor Selection in the Production of Allogeneic Memory-Like CAR NK Cells for Clinical Application
Abstract Number and Type:
128, poster
Poster Presentation Date and Time:
November 13, 2021, 7:00 am – 8:30 pm ET

* View Source; a
pre-conference program; additional registration is required.

Immunetune to Present Data on Neoantigen Cancer Vaccine Platform at SITC 2021

On October 1, 2021 Immunetune, a preclinical-stage biotech developing next-generation DNA vaccines against cancer and infectious diseases, reported the upcoming presentation of data on its neoantigen DNA cancer vaccine platform at the Society for Immunotherapy of Cancer (SITC) (Free SITC Whitepaper) Annual Meeting 2021 (Press release, ImmuneTune, OCT 1, 2021, View Source [SID1234590615]). The submitted abstract was selected for a poster presentation during the SITC (Free SITC Whitepaper) conference, taking place virtually and physically in Washington, D.C., from November 10 – 14, 2021.

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The selected abstract is titled "Personalized synthetic polyepitope DNA cancer vaccines encoding a novel pyroptotic adjuvant to generate effective anti-tumor T cell immunity". Abstracts can be accessed on the SITC (Free SITC Whitepaper) website once the conference begins on November 9; posters will be presented on November 12 and 13.

"It is an exciting opportunity to present our latest preclinical data at a leading international scientific and medical conference. Building upon our publication in the journal OncoImmunology in 2019, these data now include the combination of our synthetic, linear DNA cancer vaccine platform with a novel adjuvant that targets pyroptosis to elicit a potent T cell response against tumor-specific neoantigens," stated Jeroen van Bergen, CSO of Immunetune, and presenter of the poster at SITC (Free SITC Whitepaper).

G1 Therapeutics Announces Permanent J-Code from Centers for Medicare and Medicaid Services

On October 1, 2021 G1 Therapeutics, Inc. (Nasdaq: GTHX), a commercial-stage oncology company, reported that the permanent J-code for COSELA (trilaciclib) that was issued in July 2021 by the Centers for Medicare & Medicaid Services (CMS) is now effective for provider billing for all sites of care (Press release, G1 Therapeutics, OCT 1, 2021, View Source [SID1234590614]). The permanent J-code for COSELA, J1448 (Injection, trilaciclib, 1mg.), published online on the CMS website here (page 5).

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J-codes are permanent, product specific reimbursement codes assigned to outpatient and physician administered "buy and bill" products under Medicare Part B and are used by commercial insurers and government payers to facilitate and standardize claims submissions and reimbursements for medications like COSELA. With the permanent J-code now in effect, all hospital outpatient departments, ambulatory surgery centers and physician offices in the United States will have one consistent Healthcare Common Procedure Coding System (HCPCS) code to standardize the submission and payment of COSELA insurance claims across Medicare, Medicare Advantage, Medicaid and commercial plans.

"Given the emergent presentation of extensive-stage small cell lung cancer, and the clinical benefits of COSELA as a proactive multilineage myeloprotection drug when give prior to chemotherapy, it is absolutely essential that patients have timely access to it," said Jack Bailey, Chief Executive Officer of G1 Therapeutics. "We are pleased to receive this new permanent J-code for all sites of care as it will enable a more efficient billing process, which will ultimately help facilitate patient access to COSELA."

G1’s new technology add-on payment (NTAP) for COSELA which provides additional payment to inpatient hospitals above the standard Medicare Severity Diagnosis-Related Group (MS-DRG) payment amount also became effective for provider billing today, October 1, 2021.

About COSELA (trilaciclib) for Injection

COSELA (trilaciclib) was approved by the U.S. Food and Drug Administration on February 12, 2021.

Indication
COSELA (trilaciclib) is indicated to decrease the incidence of chemotherapy-induced myelosuppression in adult patients when administered prior to a platinum/etoposide-containing regimen or topotecan-containing regimen for extensive-stage small cell lung cancer.

Important Safety Information
COSELA is contraindicated in patients with a history of serious hypersensitivity reactions to trilaciclib.

Warnings and precautions include injection-site reactions (including phlebitis and thrombophlebitis), acute drug hypersensitivity reactions, interstitial lung disease (pneumonitis), and embryo-fetal toxicity.

The most common adverse reactions (>10%) were fatigue, hypocalcemia, hypokalemia, hypophosphatemia, aspartate aminotransferase increased, headache, and pneumonia.

This information is not comprehensive. Please click here for full Prescribing Information. View Source