Interim Results announcement for the six months ended June 30, 2022

On September 1, 2022 Alphamab reported its interim results for the six months ended June 30, 2022 (Press release, Alphamab, SEP 1, 2022, View Source [SID1234618980]).

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Jacobio Completes First Dose of IIa Clinical Trial of JAB-21822 on KRAS G12C and STK11 Co-mutation in China

On September 1, 2022 Jacobio Pharma (1167.HK) reported that the company has dosed the first non-small cell lung cancer (NSCLC) patient with KRAS G12C and STK11 co-mutation in the Phase IIa trial of KRAS G12C inhibitor JAB-21822 in China (Press release, Jacobio Pharmaceuticals, SEP 1, 2022, View Source [SID1234618957]).

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JAB-21822 is a KRAS G12C inhibitor independently developed by Jacobio utilizing the allosteric inhibitor technology, which is now used as the front-line treatment for advanced or metastatic NSCLC patients with KRAS G12C and STK11 co-mutation.

In China, there are approximately 40,000 new patients with tumors harboring KRAS G12C mutation every year. STK11 is an in-parallel biomarker of KRAS G12C. According to relevant studies, non-small cell lung cancer patients with STK11 and KRAS G12C co-mutation receiving KRAS G12C inhibitor treatment have a higher objective response rate in clinical study.

"JAB-21822 is the first and only clinical stage drug approved for first-line treatment of STK11 and KRAS G12C co-mutated non-small cell lung cancer in China. JAB-21822 is independently developed by Jacobio, which has potential to bring better treatment options to patients based on efficacy and safety," said Dr. WANG Yinxiang, Chairman and CEO of Jacobio.

JAB-21822 is the best-in-class potential project for KRAS G12C inhibitors. The preliminary clinical date of the Phase I study of JAB-21822 published at the 2022 annual meeting of American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) shows that as of April 1, 2022, a total of 72 patients with advanced solid tumors were enrolled, and efficacy was assessed for 32 NSCLC patients with KRAS G12C mutation. The overall response rate (ORR) was 56.3% (18/32) and the disease control rate (DCR) was 90.6% (29/32).

Currently, JAB-21822 is simultaneously undergoing clinical trials for monotherapy and combination therapy in China, the United States and Europe, including the monotherapy for NSCLC with KRAS G12C mutation, pancreatic ductal carcinoma and colorectal cancer; the combination therapy with EGFR monoclonal antibody; and the combination therapy with JAB-3312, a self-developed SHP2 inhibitor of the Company.

About JAB-21822

JAB-21822 is a KRAS G12C inhibitor independently developed by the Company. The Company has initiated a number of Phase I/II clinical trials in China, the United States and Europe for patients with advanced solid tumors, including monotherapy for STK11 co-mutated non-small cell lung cancer in the front-line setting; combination therapy with SHP2 inhibitor, anti-PD-1 monoclonal antibody and Cetuximab.

Prothena to Participate in Upcoming Healthcare Conferences

On September 1, 2022 Prothena Corporation plc (NASDAQ:PRTA), a late-stage clinical biotechnology company with a robust pipeline of investigational therapeutics built on protein dysregulation expertise, reported that members of its senior management team will participate in the following upcoming investor conferences (Press release, Prothena, SEP 1, 2022, View Source [SID1234618952]):

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Citi’s 17th Annual BioPharma Conference on Thursday, September 8, 1×1 investor meetings will be held
Morgan Stanley 20th Annual Global Healthcare Conference on Tuesday, September 13, a fireside chat will be held at 5:15 PM ET
H.C. Wainwright 24th Annual Global Investment Conference on Wednesday, September 14, a fireside chat will be held at 9:00 AM ET
Cantor Neurology & Psychology Conference on Thursday, October 6, 1×1 investor meetings will be held
A live webcast of the fireside chats can be accessed through the investor relations section of the Company’s website at www.prothena.com. Following the live presentation, a replay of the webcast will be available on the Company’s website for at least 90 days following the presentation date.

Y-mAbs Announces Scheduling of FDA Advisory Committee Meeting for Omburtamab

On September 1, 2022 Y-mAbs Therapeutics, Inc. (the "Company" or "Y-mAbs") (Nasdaq: YMAB) a commercial-stage biopharmaceutical company focused on the development and commercialization of novel, antibody-based therapeutic products for the treatment of cancer, reported that a meeting of the Oncologic Drugs Advisory Committee ("ODAC") of the U.S. Food and Drug Administration ("FDA") has been scheduled for October 28, 2022 to review the Company’s Biological License Application ("BLA") for its product candidate, OMBLASTYS (omburtamab), an investigational radiolabeled antibody construct (Press release, Y-mAbs Therapeutics, SEP 1, 2022, View Source [SID1234618951]). Y-mAbs resubmitted the BLA for OMBLASTYS on March 31, 2022, and the FDA assigned a Prescription Drug User Fee Act ("PDUFA") goal date of November 30, 2022, for the completion of its priority review of the OMBLASTYS BLA.

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"We look forward to the October 28, 2022 meeting with the Advisory Committee, as well as to continuing our dialogue with the FDA about OMBLASTYS and the important data, which we believe supports approval," said Thomas Gad, President, and Interim Chief Executive Officer. "This is another key step towards providing a potential treatment for pediatric patients with CNS/leptomeningeal metastasis from neuroblastoma."

Researchers at Memorial Sloan Kettering Cancer Center ("MSK") developed omburtamab, which is exclusively licensed by MSK to Y-mAbs. As a result of this licensing arrangement, MSK has institutional financial interests in the compound.

High-Grade Glioma Relapse in Children: Onxeo announces the enrollment of the first patient in the phase 1b/2 clinical study conducted by the European ITCC consortium and sponsored by Institut Curie

On September 1, 2022 Onxeo S.A. (Euronext Growth: ALONX, Nasdaq First North[1]: ONXEO), a clinical-stage biotechnology company specializing in the development of innovative drugs targeting tumor DNA Damage Response (DDR)n in particular against rare or resistant forms of cancer, reported that the first patient has been enrolled and treated in the phase 1b/2 clinical study that aims to evaluate the efficacy and tolerability of AsiDNA[2], Onxeo’s first-in-class DDR inhibitor, combined with radiotherapy in children, adolescents or young adults with relapsed High-Grade Glioma (HGG) (Press release, Onxeo, SEP 1, 2022, View Source [SID1234618877]). The clinical validation of this innovative therapy offers the hope of providing better care and treatment for these high-risk pediatric cancers.

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High Grade Gliomas (HGG), which represents approximately 20% of tumors of the central nervous system (CNS) in children, continue to have a very poor prognosis with a 5-year survival rate of less than 20%. Surgery combined with radiotherapy or chemotherapy often allows the disease to be controlled. However, this disease control is not durable due to the development of treatment-resistant tumor cells. Studies conducted in preclinical models as well as initial clinical trials conducted in adults[3] have highlighted AsiDNA’s synergetic effect when combined with treatments that target and destroy the DNA, such as radiotherapy.

This phase 1b/2 trial, sponsored by Institut Curie, is being conducted within the framework of the European ITCC[4] consortium, in order to evaluate AsiDNA’s efficacy and tolerability by enrolling a maximum of 32 patients (children, adolescents or young adults) with relapsed HGG. A first patient has been enrolled in the study at the Institut Curie’s SIREDO (Soins, Innovation, Recherche en cancérologie de l’Enfant, l’aDOlescent et l’adulte jeune, i.e. care, innovation, research in cancer in children, adolescents and young adults) Center. Additionally, other French centers as well as European countries are planned to be initiated in the coming months. The study’s first interim results are projected in the first quarter of 2024.

Shefali Agarwal, Onxeo’s President and Chief Executive Officer, stated: "Onxeo is proud of its clinical collaboration with Institut Curie, and would like to thank Professor François Doz – the study’s lead investigator – for his involvement in this project. We hope that the combination of AsiDNA and radiotherapy in this type of cancer will provide a real benefit to patients suffering from a recurrent form of high-grade glioma".

"The enrollment of the first patient is a major step in this proof-of-concept study whose goal is to evaluate the efficacy and good tolerability of the systemic administration of AsiDNA in combination with a new radiotherapy. We hope that this study will provide encouraging evidence enabling an improvement in the prognostic outcome of a disease that is a key unmet need", added Prof. François Doz, pediatric oncologist, deputy head of clinical research, innovation and teaching at Institut Curie’s SIREDO Center and this study’s lead investigator.

This phase 1b/2 study is supported by a grant from the European Fight Kids Cancer[5] program.

[1] The company reminds shareholders that the delisting of Onxeo shares from the First North Growth market in Copenhagen has been approved and the last day of trading on this market will be November 8, 2022. The company will keep its primary listing on Euronext Growth Paris.

[2] In 2016, Onxeo acquired DNA Therapeutics, a spin-off of Institut Curie building on the innovative work of Marie Dutreix, CNRS research director research at Institut Curie, which led to the development of AsiDNA.

[3] "First-in-human phase I study of the DNA repair inhibitor DT01 in combination with radiotherapy in patients with skin metastases from melanoma." Le Tourneau C et al. Br J Cancer. 2016 May 24;114(11):1199-205.

[4] The Innovative Therapies for Children with Cancer (ITCC) consortium is a non-profit organization incorporating 63 European pediatric oncology departments with expertise in conducting early-stage trials in children and adolescents and 25 European research laboratories.

[5] Fight Kids Cancer is a European call for projects, a joint initiative of France’s Imagine for Margo association, Belgium’s KickCancer foundation and Luxembourg’s Kriibskrank Kanner foundation.