IUCT-Oncopole & Artios join forces to overcome resistance to therapies for familial breast cancer

On April 13, 2023 IUCT-Oncopole reported to launch an ambitious national project in collaboration with Artios Pharma Limited (Artios), a clinical stage biotech company pioneering the development of novel small molecule therapeutics that target the DNA damage response ("DDR") process to unravel the mechanisms of resistance to anti-PARP therapies in patients with metastatic breast cancer with germline mutations of the BRCA1 and/or 2 genes (Press release, Artios Pharma, APR 13, 2023, View Source [SID1234630030]). Entitled REPARP (REpair factor expression as biomarker of PARP inhibitor resistance), its ambition is to deliver medicines that improve the survival of these patients.

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New ways to combat poor prognosis in breast cancer

Metastatic cancer occurs when the disease (tumour) has spread from the breast and local lymph nodes to other parts of the body (metastasis), such as the bones, liver or lungs. Fewer than 10% of breast cancers are metastatic at the time of diagnosis, but it is estimated that 15-20% of patients with early diagnosed breast cancer will go on to develop metastases. The aim of current metastatic treatments is to slow down the progression of a disease that unfortunately cannot be cured. Poly ADP-ribose polymerase (PARP) inhibitors are a promising new class of molecules and are prescribed alone or in combination with hormone therapy for breast cancer. This targeted therapy has reduced the risk of relapse in patients with a BRCA1 and/or 2 mutation in both the metastatic and early stages. However, at the metastatic stage, some patients present a disease that is resistant to this treatment from the outset or eventually develop resistance, i.e. their disease progresses despite the treatment.

BRCA1 and BRCA2 play a major role in a pathway for repairing chromosomal breaks known as homologous recombination. They act like ‘mechanics’ in our cells. In the case of BRCA1 and/or 2 mutations, this repair pathway is impaired. PARP inhibitors act by increasing the rate of breaks leading to tumour cell death. PARP is a major player in the alternative DNA repair pathways used by cancer cells for survival in the case of BRCA1 and/or 2 mutations.
Recent laboratory studies suggest that tumour cells resistant to PARP inhibitors set up another alternative repair pathway mediated by the DNA Polymerase or POLQ, which acts as a substitute ‘mechanic’. POLQ inhibitors being developed by Artios (Phase I underway; NCT04991480) could prevent or treat this resistance to PARP inhibitors.

The IUCT-Oncopole’s and Artios’ expertise in translational research underpins the REPARP project.

The REPARP project consists of using tumour and fluid samples (blood samples) taken at different times during treatment with PARP inhibitors to explore whether the POLQ repair pathway is established and is associated with therapeutic resistance. This would allow the identification of patients who could
benefit from further treatment with POLQ inhibitors. The aim is to include 120 patients throughout the 25 national centres participating in the study. Results are expected in three years.

"PARP inhibitors have significantly improved the treatment of cancers, but long-term use can often lead to resistance that is challenging to overcome," said Prof. Florence Dalenc Department of Medical Oncology The IUCT-Oncopole. "Analyzing tumour samples can help us better understand why some patients experience a lack of efficacy to PARP inhibitors. These learnings can help improve treatment decisions for different patient types and help determine potential drug combinations with synergistic activity that can restore sensitivity to PARP inhibition."

Prof. Florence Dalenc (Department of Medical Oncology), and Drs. Jean-Sébastien Hoffmann and Camille Franchet (Department of Anatomy and Pathologic Cytology – CHU de Toulouse, directed by Prof. Pierre Brousset) are coordinating this study. Pathological and imaging analyses are carried out by the Imag’IN platform (View Source) coordinated by Drs. François-Xavier Frenois and Nathalie Van Acker. The translational part on liquid biopsy (obtained from blood) is undertaken by the team directed by Dr. Anne Pradines (Laboratory of Oncological Medical Biology) and is funded by the National Cancer Institute (INCa).

The translational and bioinformatics team at Artios, led by Dr. Sarah Holt and Dr. Suraj Menon respectively, will also be heavily involved in the analysis of the liquid and tumour biopsy samples using the Artios DcoDeR Platform.

Allogene Therapeutics Announces Participation in Four Upcoming Investor Conferences

On April 13, 2023 Allogene Therapeutics, Inc. (Nasdaq: ALLO), a clinical-stage biotechnology company pioneering the development of allogeneic CAR T (AlloCAR T) products for cancer, reported that it will participate in four upcoming investor conferences (Press release, Allogene, APR 13, 2023, View Source [SID1234630029]).

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Canaccord Genuity – CG Horizons in Oncology Virtual
Thursday, April 20, 2023
8:00AM PT/11:00AM ET

BofA Securities 2023 Health Care Conference
Wednesday, May 10, 2023
4:20PM PT/7:20PM ET

The JMP Securities Life Sciences Conference
Monday, May 15, 2023
8:30AM PT/11:30AM ET

2023 RBC Capital Markets Global Healthcare Conference
Tuesday, May 16, 2023
1:35PM PT/4:35PM ET

Any available webcasts will be posted to the Company’s website at www.allogene.com under the Investors tab in the News and Events section. Following a live webcast, a replay will be available on the Company’s website for approximately 30 days.

ALENTIS THERAPEUTICS CLOSES $105 MILLION SERIES C FUNDING TO ADVANCE TRANSFORMATIONAL MEDICINES FOR CLAUDIN-1

On April 13, 2023 Alentis Therapeutics ("Alentis"), the Claudin-1 (CLDN1) company, reported $105 million in Series C financing (Press release, Alentis Therapeutics, APR 13, 2023, View Source [SID1234630028]). The funding round was led by Jeito Capital together with Novo Holdings A/S and RA Capital Management with participation from existing investors including BB Pureos Bioventures, Bpifrance through its InnoBio 2 fund and Schroders Capital.

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The financing will support Phase II and Phase I programs of Alentis’ lead investigational products ALE.F02 and ALE.C04 respectively as well as the CLDN1 platform development.

"We are absolutely delighted with this support from our investors," said Dr. Roberto Iacone, CEO at Alentis Therapeutics. "There are huge unmet needs in organ fibrosis and cancer, and this funding enables us to continue with the important work we’re doing in the CLDN1 space and generate clinical data from both our programs. We can now aggressively develop CLDN1 biology in oncology and continue with the recruitment of our organ fibrosis trials while advancing our ADC and bi-specific antibodies."

Founder and CEO of Jeito Capital, Rafaèle Tordjman said, "We are totally convinced about the CLDN1 biology potential in multiple areas of fibrosis and oncology. Alentis has made significant progress in identifying target populations while developing programs and advancing the platform. We are committed to continuing our partnership with Alentis as they are the leading player in the CLDN1 space and are well positioned to generate meaningful clinical data within the next 1218 months."

Novo Holdings’ Senior Partner, Naveed Siddiqi will join the Alentis Therapeutics’ Board of Directors. "The Venture Investments team of Novo Holdings has an extensive track record of backing high-quality biotechs across Europe and the US developing novel treatments for unmet medical needs," said Naveed Siddiqi. "Alentis has pioneered a world-leading position in the Claudin-1 space and is led by highly capable drug developers. We were encouraged by exciting emerging preclinical data in oncology and the potential of Claudin-1 targeted therapeutics to treat a wide range of cancers where Claudin-1 is highly expressed. We are looking forward to supporting Alentis as it further advances its pipeline in the clinic with the proceeds of this round."

Since its $67 million Series B funding in June 2021, Alentis has made major strides: ALE.F02 MAD study completion is imminent; it has clearly defined the CLDN1+ cancer patient population, including T-cell excluded cancers to develop ALE.C04 in oncology; set-up the platform to engineer CLDN1 antibody drug conjugates and bispecific antibodies that the Series C will help to further develop; and is expanding its team of top talent.

Nkarta to Participate at Upcoming Investor Conferences

On April 12, 2023 Nkarta, Inc. (Nasdaq: NKTX), a biopharmaceutical company developing engineered natural killer (NK) cell therapies to treat cancer, reported its participation at two upcoming investor conferences (Press release, Nkarta, APR 13, 2023, View Source [SID1234630001]):

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22ND Annual Needham Virtual Healthcare Conference
April 17, 2023
3:00 p.m. ET – fireside chat

Canaccord Genuity Horizons in Oncology Virtual Conference
April 20, 2023
3:00 p.m. ET – panel discussion

A simultaneous webcast of each event will be available on the Investors section of Nkarta’s website, www.nkartatx.com, and a replay will be archived on the website for approximately 90 days.

Araris Biotech AG Announces Strategic Investment with Samsung Ventures

On April 12, 2023 Araris Biotech AG ("Araris" or "the Company"), a company pioneering a proprietary antibody-drug conjugate (ADC)-linker technology, reported that Samsung Venture Investment Corporation ("Samsung Ventures"), an investment corporation established to promote the development of new technologies, has invested in the Company in an independent deal ahead of its on-going series A funding (Press release, Araris Biotech, APR 12, 2023, View Source [SID1234651280]).

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The investment was made via Samsung Life Science Fund – created jointly between Samsung Biologics (KRX: 207940.KS) and Samsung C&T, and managed by Samsung Ventures – which reflects Samsung’s commitment to further explore and expand various business opportunities in biopharmaceuticals.

Araris Biotech is a company pioneering a proprietary antibody-drug conjugate (ADC)- linker technology, where its linker platform enables payload attachment to off the shelf antibodies without needing to re-engineer or reduce antibodies, resulting in highly homogenous, stable and potent ADC therapies in a cost and time efficient manner. It also has the potential to address challenges associated to ADCs, including solubility and unstable linkage issues.

The latest investment reflects Samsung’s commitment to further expanding its pipeline. Samsung, as a strategic investor, will collaborate on evaluating, manufacturing and developing assets with Araris using the Company’s proprietary ADC Technology, in close collaboration with Samsung affiliates involved in the discovery and development, and manufacturing of novel biologics.

"Araris has the potential to develop best-in-class ADC therapies, and we see room for collaboration in the manufacturing and development of new drugs," said John Rim, CEO of Samsung Biologics.

"We’re pleased to receive this support from Samsung, as well as the recognition of the potential of our linker-payload toolbox and conjugation technology in such a quickly growing ADC field," said Philipp Spycher, Ph.D., chief executive officer and co-founder of Araris Biotech. "We look forward to using these proceeds to further support our efforts in advancing our ADC candidates toward the clinic."