Lyell Immunopharma to Participate in Goldman Sachs Global Healthcare Conference

On June 7, 2022 Lyell Immunopharma, Inc., (Nasdaq: LYEL), a clinical-stage T-cell reprogramming company dedicated to developing curative cell therapies for patients with solid tumors, reported that members of its senior management team will participate in the Goldman Sachs 43rd Annual Global Healthcare Conference on Tuesday, June 14 at 10:40am PT (Press release, Lyell Immunopharma, JUN 7, 2022, View Source [SID1234615701]).

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A live webcast of the fireside chat can be accessed through the investor relations section of the Company’s website at www.lyell.com. Following the live presentation, a replay of the webcast will be available on the Company’s website for 90 days following the presentation date.

Ichnos Sciences To Present At The 2022 Jeffries Healthcare Conference

On June 7, 2022 Ichnos Sciences Inc., a clinical-stage global biotechnology company developing innovative multispecific antibodies for oncology, reported that its president and chief executive officer, Cyril Konto, M.D., will present at the 2022 Jefferies Healthcare Conference in New York on Wednesday, June 8 at 3:30 PM Eastern Time (Press release, Ichnos Sciences, JUN 7, 2022, View Source [SID1234615699]).

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"Ichnos has been working to develop and advance therapies for cancer that extend and improve survival and quality of life, driven by the belief that cure is possible," said Cyril Konto, M.D., President and Chief Executive Officer of Ichnos Sciences. "We are excited to come together with other health and biotech innovators at the Jefferies Conference and honored to have the opportunity to share our plans for shifting medicine forward."

Dr. Konto’s presentation comes just weeks after Ichnos announced the selection of its ISB 2001 TREAT[1] trispecific antibody, the first T cell-engaging antibody that targets BCMA and CD38 on multiple myeloma cells, as its next candidate to move into clinical development. Ichnos’ pipeline also includes ISB 1342, a CD38 x CD3 bispecific antibody, which continues to enroll patients with relapsed/refractory multiple myeloma in an ongoing Phase 1, dose escalation and expansion study, and ISB 1442, a CD38 x CD47 biparatopic bispecific antibody for which a Phase 1 study in relapsed/refractory multiple myeloma is planned to start shortly.

A live webcast of the presentation can be accessed through this link. A replay of the webcast will be available for one year following the conference.

FORUS Therapeutics Inc (“FORUS”) Announces XPOVIO® (selinexor) Is Authorized for Sale by Health Canada

On June 7, 2022 FORUS Therapeutics Inc ("FORUS"), reported that on May 31, 2022 XPOVIO (selinexor) was authorized for sale by Health Canada in combination with bortezomib and dexamethasone for the treatment of adult patients with multiple myeloma (MM) who have received at least one prior therapy (Press release, FORUS Therapeutics, JUN 7, 2022, View Source;utm_medium=rss&utm_campaign=forus-therapeutics-inc-forus-announces-xpovio-selinexor-is-authorized-for-sale-by-health-canada [SID1234615698]).

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Approval was based on the Phase 3 BOSTON trial of XPOVIO in combination with once-weekly bortezomib and low-dose dexamethasone compared to twice-weekly bortezomib and low-dose dexamethasone in patients with relapsed or refractory multiple myeloma.
This is the first regulatory approval for XPOVIO in Canada in multiple myeloma and follows recent approvals in Australia, China, South Korea, Singapore and the United States.
XPOVIO is a first-in-class, oral Selective Inhibitor of Nuclear Export (SINE) compound.
"The FORUS team is very proud to launch XPOVIO in Canada and bring forth a novel and effective addition to existing regimens for the treatment of relapsed or refractory multiple myeloma. This first approval is just the beginning of our journey to fulfill our company’s mission and vision. We are moving quickly to ensure Canadian MM patients have broad, equitable access to XPOVIO." said Kevin Leshuk, President and CEO of FORUS.

"The approval of XPOVIO brings an exciting new anti-myeloma agent with a novel mechanism of action into the treatment armamentarium for relapsed multiple myeloma," says Dr. Donna Reece, Professor and Director of the Program for Multiple Myeloma and Related Diseases in the Department of Medical Oncology and Hematology at Princess Margaret Cancer Centre/University of Toronto, Chief Medical Officer and Director of the Canadian Myeloma Research Group (CMRG). "Treating multiple myeloma is not a one-size-fits-all approach and the approval of XPOVIO in combination with bortezomib and dexamethasone will allow clinicians to further tailor their treatment strategies to meet the unique needs of each individual patient. In addition, the CMRG and Canadian patients played a significant role in the clinical development of XPOVIO, and it is rewarding to see these efforts result in a Health Canada approval."

About Multiple Myeloma
Multiple myeloma (MM), commonly referred to as myeloma, is a blood cancer that is associated with the abnormal behavior and uncontrolled growth of a type of white blood cell – the plasma cell. Plasma cells are made in the bone marrow – the spongy tissue found inside bones – and are an important component of the body’s immune system because they produce antibodies. In myeloma, abnormal plasma cells (also known as myeloma cells) interfere with the production of normal healthy blood cells in the bone marrow and overproduce inactive clones of abnormal antibodies that can negatively affect different parts of the body such as the bones and kidneys. The cause or causes of myeloma remain unknown.

In Canada, it is estimated that in 2022 approximately 4,000 people will be diagnosed with multiple myeloma, and almost 12,500 Canadians are living with MM at any given time. Despite recent introductions of newer, effective treatments, MM remains an incurable, deadly disease with an estimated 5-year net survival rate of 50%. These facts reinforce the continued need for new treatments that can contribute to controlling the disease and extend patient benefits.

Martine Elias, MSc, Executive Director, Myeloma Canada states "New treatment options for the Myeloma patient community are incredibly important as this disease remains incurable and each patient has very unique needs due to the disease and other health conditions. The approval of XPOVIO in combination with bortezomib and dexamethasone is a very welcomed addition to the treatment options for Canadian MM patients as it provides patients with a unique, effective oral option that seems to be very well tolerated when used appropriately."

About XPOVIO (selinexor)
XPOVIO is the first and only oral XPO1 inhibitor available for the treatment of multiple myeloma. Its unique mechanism acts by blocking the nuclear export protein XPO1 which can promote the intranuclear accumulation and activation of tumor suppressor proteins and growth regulating proteins, and down-regulate the levels of multiple oncogenic proteins. Due to this novel mechanism of action, XPOVIO is being evaluated for use in multiple combination regimens.

XPOVIO is a registered trademark of Karyopharm Therapeutics Inc. and is used by FORUS Therapeutics Inc. under license.

ImmunOs Therapeutics Raises $74 Million Series B Financing Round

On June 7, 2022 ImmunOs Therapeutics AG, a biopharmaceutical company leveraging its HLA-based technology platform to develop first-in-class therapeutics for the treatment of cancer and autoimmune diseases, reported the closing of an oversubscribed Series B financing round totaling $74 million (Press release, ImmunOs Therapeutics, JUN 7, 2022, View Source [SID1234615697]). The round was led by new investors Samsara BioCapital, Lightspeed Venture Partners, and Gimv, and joined by new investors Mission BioCapital, GL Capital, PEAK6 Strategic Capital, and Fiscus Financial, as well as existing investors Pfizer Ventures, BioMed Partners, and Schroder Adveq. In connection with the financing, Shelley Chu, MD, PhD, Partner at Lightspeed, Marcos Milla, PhD, Venture Partner at Samsara, and Andreas Jurgeit, PhD, Partner at Gimv, will join the Company’s Board of Directors, which currently includes Reinhard Ambros, PhD, Chairperson and former Head of the Novartis Venture Fund, Daniel Vasella, MD, Vice Chairperson and former Chairperson and CEO of Novartis AG, Markus Hosang, PhD, General Partner at BioMed Partners, Michael Baran, PhD, Partner at Pfizer Ventures, and Sean R. Smith, CEO of ImmunOs.

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The proceeds of the Series B will be used to fund the clinical development of ImmunOs’ lead program, IOS-1002 (formerly iosH2), through Phase 2 clinical trials and to progress additional oncology and autoimmune disease programs within the Company´s HLA-based pipeline towards clinical development. IOS-1002 is a first-in-class, multi-functional agent based on a naturally occurring human leukocyte antigen (HLA) that targets key components of the innate immune system, including LILRB1 (ILT2), LILRB2 (ILT4), and KIR3DL1, and synergizes with the adaptive immune system, thereby leading to profound anti-tumor activity. A Phase 1 clinical trial is planned to start in the second half of 2022.

Additionally, ImmunOs has established a U.S. subsidiary to further expand its international reach, execute future U.S. clinical trials, and strengthen its transatlantic operations and team.

"We are delighted to close this significant financing round led by a group of top-tier U.S. and European investors," said Sean R. Smith, CEO of ImmunOs Therapeutics. "The raise underlines our promising, first-in-class immunotherapy approach for the treatment of both solid and liquid tumors. The funding allows us to advance our lead program, IOS-1002, into clinical trials, expand our pipeline in oncology and autoimmune disease, and strengthen our transatlantic operations. We are honored that renowned investors such as Samsara, Lightspeed, Gimv, Mission BioCapital, GL Capital, PEAK6, and Fiscus have joined our investor base."

"We are excited to invest in ImmunOs Therapeutics with its innovative HLA-based technology platform, expert leadership team, and strong syndicate of investors," said Shelley Chu, MD, PhD, Partner at Lightspeed Venture Partners. "The Company is ideally positioned to advance its potentially first-in-class immunotherapies for the benefit of patients with limited therapeutic options. We look forward to supporting ImmunOs’ success."

"Myeloid checkpoint therapeutics are potentially the next major breakthrough in immuno-oncology, and we believe ImmunOs Therapeutics will contribute exciting medicines in this rapidly evolving field to help patients suffering from cancer," continued Marcos Milla, PhD, Venture Partner at Samsara. "We look forward to generating data from the initial clinical trials of IOS-1002."

"ImmunOs’ approach of identifying HLA molecules with naturally optimized affinity and specificity profiles is not just elegant but also truly differentiated – a novel modality leveraging the co-evolution of immune-regulatory mechanisms," stated Andreas Jurgeit, PhD, Partner at Gimv. "We are extremely excited by the progress being made at ImmunOs and proud to support the team towards clinical validation for the benefit of patients."

Crinetics Pharmaceuticals to Participate in the JMP Securities Life Sciences Conference

On June 7, 2022 Crinetics Pharmaceuticals, Inc. (Nasdaq: CRNX), (Nasdaq: CRNX), a clinical-stage pharmaceutical company focused on the discovery, development, and commercialization of novel therapeutics for rare endocrine diseases and endocrine-related tumors, reported that company management will participate in person in a fireside chat at the annual JMP Securities Life Sciences Conference, which is being held at the Lotte New York Palace on June 15-16, 2022 (Press release, Crinetics Pharmaceuticals, JUN 7, 2022, View Source [SID1234615696]).

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In addition, the live and archived presentation will be accessible on the Events & Presentations page in the Investors section on the Company’s website.