Nerviano Medical Sciences S.r.l. Shared Data on NMS-01940153E selected for Oral Presentation at 34th EORTC-NCI-AACR Symposium on Molecular Targets and Cancer Therapeutics 

On October 28, 2022 Nerviano Medical Sciences Srl (Company), a member of NMS Group and a clinical stage company discovering and developing innovative therapies for the treatment of cancer, reported that data from the Company’s Phase I/II clinical study of NMS-01940153E in Hepatocellular carcinoma (HCC) in an oral presentation by Dr. Maria Reig at the EORTC-NCI-AACR (Free EORTC-NCI-AACR Whitepaper) Symposium on Molecular Targets and Cancer Therapeutics (ENA 2022) in Barcelona (Press release, Nerviano Medical Sciences, OCT 28, 2022, View Source [SID1234623261]).

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Fosun Kite’s NDA Accepted for Second Indication of CAR-T in China

On October 28, 2022 Shanghai Fosun Kite reported China’s NMPA has accepted its NDA filing of the company’s CAR-T as a second-line therapy for large B cell lymphoma. One year ago, Yikaida was approved for third-line use in the same disease (Press release, Fosun Kite Biotechnology, OCT 28, 2022, View Source [SID1234622594]). Fosun Kite is a joint venture tasked with bringing Kite’s Yescarta to China. The drug, axicabtagene ciloleucel, is an autologous CD19 CAR T-cell therapy manufactured in China under a Kite license. The new indication will be for adult patients with large B cell lymphoma who did not respond to first-line immunochemo therapy or who relapsed within 12 months.

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Marengo Therapeutics Presents Preclinical Proof-of Concept Data for STAR0602, a First-in-class Selective T cell Activator, at the 34th EORTC-NCI-AACR Symposium 2022

On October 28, 2022 Marengo Therapeutics, Inc., a company pioneering novel therapeutics targeting the T cell receptor Vβ chain (TCR Vβ) to selectively activate the right T cell subsets to fight cancer, reoorted the first preclinical proof-of-concept data on STAR0602, its novel TCR agonist antibody, during the 34th EORTC-NCI-AACR (Free EORTC-NCI-AACR Whitepaper) Symposium on molecular targets and cancer therapeutics (ENA) in Barcelona, Spain (Press release, Marengo Therapeutics, OCT 28, 2022, View Source [SID1234622588]). The data presented showed potent anti-tumor activity of STAR0602 in a range of solid tumor models, including those refractory to check point inhibitors like PD-1/PD-L1.

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The plenary oral presentation was given by James Gulley, M.D., Ph.D., Co-Director of the Center of Immuno-Oncology (CIO), Deputy Director of the Center for Cancer Research (CCR) at the National Cancer Institute (NCI), and acting Clinical Director, NCI.

"STAR0602 offers an entirely new mechanism of selective T cell activation that increases both the quantity and quality of T cell responses to the tumor via a mechanism that is distinct to checkpoint inhibitors," said Zhen Su, M.D., MBA, Chief Executive Officer of Marengo. "These results strongly suggest our lead asset has the potential to become a next-generation IO backbone treatment against a range of solid tumors representing a novel therapeutic strategy for patients."

"We are pleased to share the first data for our STAR0602 program," added Andrew Bayliffe, Ph.D., Chief Scientific Officer of Marengo. "These studies show that our selective Vβ T cell activators access novel T cell immunology that has the potential to fundamentally remodel the adaptive immune response to solid tumors and install long-term tumor immunity."

Across a range of refractory murine syngeneic solid tumor models, mSTAR0602 (the murine surrogate of STAR0602) monotherapy at moderate dose levels either eradicated tumors or led to substantial regressions – effects that were durable over the long term. mSTAR0602-cured mice also showed long-term protection from tumor re-challenge. This anti-tumor activity was shown to be dependent on the accumulation of a specific subset of Vβ T cells in tumors that adopt a novel effector memory phenotype and a striking increase in TCR diversity. The expansion of these effector memory Vβ T cells was accompanied by a reduction in exhausted T cells and regulatory T cells. Similar potent expansion of human TILs and tumor killing was observed in primary syngeneic human ex vivo tumor models derived from several patient samples. The anti-tumor activity of STAR0602 in these ex vivo human tumor models was superior to pembrolizumab when tested in parallel at therapeutic concentrations.

Additional presentation details are outlined below:

Title: STAR0602, a novel TCR agonist antibody, demonstrates potent anti-tumor activity in refractory solid tumor models through the expansion of a novel, polyclonal effector memory T cell subset
Abstract Number: ENA22-0183
Session Day/Time: Friday, October 28; 12:40 pm, CET
Location: Barcelona International Convention Center, Barcelona, Spain
Presenter: James Gulley, M.D., Ph.D.
Research Highlights:
Non-human primate and patient organoid studies were conducted to confirm translation of STAR0602 target immunology to support planned human clinical trials.
The START-001 clinical study will assess the safety, tolerability, and preliminary clinical activity of STAR0602 as a single agent in patients with advanced antigen-rich solid tumors including PD-1 refractory patients. This open label, multicenter Phase 1/2 study consists of two parts: Phase 1 dose escalation and Phase 2 dose expansion. For more information, please visit clinicaltrials.gov (trial identifier: NCT05592626)

Hinova Disclosed the Preclinical Results of HP518 (Oral AR PROTAC) at the 5th Annual TPD Summit

On October 28, 2022 Hinova Pharmaceuticals Inc. (STAR: 688302), a clinical-stage biopharmaceutical company focused on developing novel therapeutics for cancers and metabolic diseases through targeted protein degradation technologies, reported their preclinical results of HP518, an orally bioavailable chimeric degrader targeting androgen receptor (AR) for prostate cancer treatment, at the 5th Annual TPD Summit (Press release, Hinova Pharmaceuticals, OCT 28, 2022, View Source [SID1234622587]).

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Discovered and developed by Hinova, HP518 showed high degradation activity against fl-AR and most enzalutamide resistant AR point mutants, and demonstrated excellent antiproliferation activities against prostate cancer cell lines. Meanwhile, HP518 exhibited good metabolic stability and is stable in human plasma. HP518 showed excellent antitumor efficacy in xenograft model by oral dosing. HP518 was also well tolerated in preclinical tox studies.

HP518 is currently in Phase-I clinical trials in Australia. The ongoing open-label clinical study will evaluate the safety, pharmacokinetics, and anti-tumor activity of HP518 in patients with metastatic castration-resistant prostate cancer (mCRPC).

"Existing data makes us more confident that HP518 has the potential to be an innovative clinical option to patients with mCRPC," said Xinghai Li, MD/Ph.D., Chief Science Officer of Hinova, "Considering prostate cancer is a progressive disease, we have established a strong pipeline targeting the androgen receptor pathway for prostate cancer treatment. Based on our targeted protein degradation drug discovery platform, we are committed to develop best-in-class and first-in-class medicines to address unmet medical needs."

Hinova has established a targeted protein degradation drug discovery platform, which allows Hinova to integrate TPD biology and medicinal chemistry and to identify and optimize chimeric degraders with high efficiency. Furthermore, Hinova has accumulated much experience in development of Chimeric degrader.

Flare Therapeutics Presents Comprehensive Real-World Data in Advanced and Metastatic Urothelial Cancer in Support of Therapeutic Targeting of PPARG at 2022 EORTC-NCI-AACR Symposium

On October 28, 2022 Flare Therapeutics, a biotechnology company targeting transcription factors to discover precision medicines for cancer and other diseases, reported that translational insights from a retrospective advanced urothelial cancer (UC) cohort in a poster titled, "Peroxisome Proliferator-Activated Receptor Gamma (PPARG) status defines the luminal lineage in molecular profiles of advanced urothelial cancers (UC)" at the 34th EORTC-NCI-AACR (Free EORTC-NCI-AACR Whitepaper) Symposium, being held in Barcelona, Spain (Press release, Flare Therapeutics, OCT 28, 2022, View Source [SID1234622586]). Molecular RWD, comprising of more than 3,000 genomic and transcriptomic profiles from advanced UC tissue, were utilized to evaluate the transcription factor PPARG, and its role as a master regulator of the luminal lineage associated with its expression and mutational status.

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"To the best of our knowledge, this represents the largest RWD from patients with advanced and metastatic urothelial cancer, providing unique insights into the persistence of PPARG signaling through disease progression, independent of the treatment paradigm," said Michaela Bowden, Ph.D., Senior Vice President of Biology and Translation at Flare Therapeutics. "Stratification of patients based upon their PPARG status serves as the foundation for our precision approach in identifying individuals most likely to respond to PPARG inhibition."

Flare presented its novel PPARG program demonstrating robust preclinical activity in a poster presentation titled, "Novel inhibitors of the luminal lineage transcription factor peroxisome proliferator-activated receptor gamma (PPARG) durably eradicate tumors in urothelial cancer animal models" on Wednesday, October 26th at same symposium.

Data highlights:

65% of advanced urothelial cancers evaluated were classified as luminal, of which one in three were enriched for genetic alterations in PPARG, RXRA or FGFR3
PPARG amplification, including a gain of only one copy number, is associated with higher PPARG expression
PPARG expression levels were sustained in metastatic lesions compared locally advanced tissues and did not significantly vary by metastatic tissue site
Flare is advancing a novel PPARG inhibitor through Investigational New Drug (IND)-enabling studies and expects to initiate its Phase 1 clinical trial in 2023 in individuals with locally advanced or metastatic UC.

About Advanced Urothelial Cancer
Muscle-invasive UC is a common type of bladder cancer, with about 20,000 individuals diagnosed each year in the United States alone, and significantly higher incidence rates in other regions of the world. This disease has high rates of recurrence and the five-year survival rate is approximately 5% in metastatic cases. The transcription factor peroxisome proliferator-activated receptor gamma (PPARG) is associated with the luminal lineage subtype reflecting approximately 65% of all advanced UC patients. Recurrent genetic alterations in PPARG, including focal amplification, missense mutations, and fusions, as well as hotspot mutations in its binding partner, retinoid X receptor alpha (RXRA) are characteristic of this molecular subtype.