Protagonist Therapeutics to Host Investor Conference Call and Webcast to Discuss Updated Phase 2 Rusfertide Results in Polycythemia Vera as Presented at EHA 2021

On June 27, 2021 Protagonist Therapeutics (Nasdaq: PTGX) ("Protagonist" or "the Company") reported that management will host an investor conference call and webcast to provide a brief corporate update and discuss data from its ongoing Phase 2 clinical study evaluating rusfertide in polycythemia vera (PV), which was selected as an oral presentation at the European Hematology Association (EHA) (Free EHA Whitepaper) 2021 Annual Congress (Press release, Protagonist, JUN 7, 2021, View Source [SID1234583688]). The conference call will take place on Friday, June 11, 2021, at 8:00 a.m. EDT (14:00 CEST).

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The call will feature members of the Protagonist management team and Ronald Hoffman, M.D., Albert A. and Vera G. List Professor of Medicine, Hematology and Medical Oncology, and Director of the Myeloproliferative Disorders Research Program at Mount Sinai Hospital, and a lead investigator of the Phase 2 study.

Featured Abstract

Rusfertide (PTG-300) Eliminates the Need for Therapeutic Phlebotomy in Both Low and High-Risk Polycythemia Vera (PV) Patients (S200; Kremyanskaya, et al). The oral presentation will be made available on demand to registered meeting attendees at ehaweb.org on Friday, June 11, 2021 at 9:00 CEST.

Conference Call and Webcast Information

Live audio of the conference call will be simultaneously broadcast over the internet. The call will be available to investors, members of the news media, and the general public.

To access the live call, dial (877) 870-4263 (U.S./Canada) or (412) 317-0790 (international) five minutes prior to the call and ask to be joined to the Protagonist Therapeutics call. A live and archived webcast will be accessible in the Investors section of the Company’s website at www.protagonist-inc.com.

Study of Paxalisib in Primary CNS Lymphoma at Dana-Farber Cancer Institute Enrols First Patient

On June 7, 2021 Kazia Therapeutics Limited (NASDAQ: KZIA; ASX: KZA), an oncology-focused drug development company, reported that a phase II study of Kazia’s investigational new drug, paxalisib, in primary CNS lymphoma has been initiated at Dana-Farber Cancer Institute, with the first patient successfully enrolled to the study (Press release, Dana-Farber Cancer Institute, JUN 7, 2021, View Source [SID1234583687]).

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Key Points

Lymphoma is a cancer of white blood cells. It occurs in the lymphatic system and can spread almost anywhere in the body; primary CNS lymphoma (PCNSL) occurs exclusively in the brain and central nervous system
The PI3K inhibitor class, to which paxalisib belongs, is well validated in lymphoma outside the brain; three of the four FDA-approved PI3K inhibitors are treatments for forms of lymphoma, but they are assumed ineffective for PCNSL since they cannot cross the blood-brain barrier
DFCI study (NCT04906096) is an open-label phase II clinical trial of paxalisib in PCNSL, and is expected to recruit up to 25 patients, taking up to 2 years to complete
Kazia will provide support including study drug and a financial grant
Dana-Farber Cancer Institute (DFCI) is a world-leading cancer treatment and research centre, based in Boston, Massachusetts. It is a principal teaching affiliate of Harvard Medical School and has been designated a Comprehensive Cancer Center by the US National Cancer Institute. DFCI participates in as many as 600 clinical trials at any given time and has been an important contributor to the development of many important new cancer therapies.

The Principal Investigator for the study, Dr Lakshmi Nayak, commented "our center has a strong research focus in primary CNS lymphoma. We are very interested to explore the potential for a brain-penetrant PI3K inhibitor in this disease. Patient outcomes in PCNSL remain far from optimal, and there is a pressing need for new treatment options."

Kazia CEO, Dr James Garner, commented, "we are delighted to see this study underway, and congratulate Dr Nayak and her team on getting it launched. With paxalisib now in an international pivotal study for glioblastoma, we are increasingly focused on identifying other groups of patients who may benefit from the drug. There is a very sound rationale to explore PCNSL in this disease, and we are looking forward to seeing the study progress."

Primary CNS Lymphoma

Lymphoma is a haematological malignancy (blood cancer) that originates from lymphocytes, a type of white blood cell involved in the immune system. PCNSL is a specific form of the disease that originates in the brain and central nervous system.

Three of the four PI3K inhibitors approved by the US Food and Drug Administration (FDA) are treatments for various forms of lymphoma, provide a strong validation for PI3K as a target in this disease. Paxalisib is the only PI3K inhibitor in mainstream development with the ability to penetrate the blood-brain barrier, and as such has a unique rationale for development in PCNSL.

The incidence of PCNSL has been increasing with time. Patients are typically in their 60s or older, and the disease is slightly more common in men.[1] The mainstays of treatment comprise chemotherapy and radiotherapy, but recurrence is common and only approximately 30% of patients remain alive five years after diagnosis.[2] Many of the drugs used to treat lymphoma elsewhere in the body are ineffective in PCNSL due to their inability to cross the blood-brain barrier.

DFCI Clinical Trial

The CNS Lymphoma Center (CNSLC) at Dana-Farber / Brigham and Women’s Cancer Center is the first centre of its kind in the world dedicated to providing comprehensive care and research for patients with primary or secondary CNS lymphoma. With the most advanced treatment options available — including surgery, chemotherapy, stem cell transplant, radiation therapy, immunotherapy, and targeted therapies, and with extensive clinical trial options — CNSLC is uniquely qualified to treat patients with CNS lymphoma and advance the outcome of patients with these tumors.

The principal investigator for the study is Dr Lakshmi Nayak, Director of the CNS Lymphoma Center at Dana-Farber Cancer Institute. Dr Nayak is an Assistant Professor of Neurology at Harvard Medical School and a board-certified neuro-oncologist. Her research interests focus on metastatic brain cancer, glioblastoma, and PCNSL, and she is extensively published in the field of brain cancer. She has been an investigator for multiple clinical trials of experimental drugs in this disease area.

Paxalisib Clinical Program

The initiation of this trial in PCNSL brings the number of ongoing clinical studies of paxalisib in brain cancer to eight.

Sponsor

Phase

Indication

Registration

Kazia Therapeutics

II

Glioblastoma

NCT03522298

Global Coalition for
Adaptive Research

II / III

Glioblastoma

NCT03970447

Alliance for Clinical Trials
in Oncology

II

Brain metastases

NCT03994796

Dana-Farber Cancer
Institute

II

Breast cancer brain metastases

(with Herceptin)

NCT03765983

Dana-Farber Cancer
Institute

II

Primary CNS lymphoma

NCT04906096

Pacific Pediatric Neuro-
Oncology Consortium

N/A

DIPG & DMGs

TBD

St Jude Children’s
Research Hospital

I

DIPG (childhood brain cancer)

NCT03696355

Memorial Sloan Kettering
Cancer Center

I

Brain metastases

(with radiotherapy)

NCT04192981

Lipocine to Present at the Lytham Partners Summer 2021 Investor Conference

On June 7, 2021 Lipocine Inc. (NASDAQ: LPCN), a clinical-stage biopharmaceutical company focused on metabolic and endocrine disorders, reported that the Company will present at the Lytham Partners Summer 2021 Investor Conference (Press release, Lipocine, JUN 7, 2021, View Source [SID1234583686]). The conference will be held virtually. Presentation details are below.

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Lytham Partners Summer 2021 Investor Conference June 14-16

Presentation time:

June 14, 2021 starting at 3:30 PM ET

Webcast link:

View Source

The webcast of this presentation will also be available on Lipocine’s corporate website under "Events & Presentations" in the Investors section.

Servier Presents Updated Translational Data from Perioperative Study of Vorasidenib and TIBSOVO® (ivosidenib tablets) in Patients with IDH Mutant Low-Grade Glioma at ASCO 2021

On June 7, 2021 Servier, a growing leader in oncology committed to bringing the promise of tomorrow to the patients we serve, reported updated data from an ongoing perioperative study confirming robust biomarker suppression and reduced tumor cell proliferation with treatment of single-agent vorasidenib and TIBSOVO (ivosidenib tablets) in low-grade glioma with an IDH1 mutation (Press release, Servier, JUN 7, 2021, View Source [SID1234583685]). The data were featured in an oral presentation at the 2021 American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) annual meeting, which is being held virtually.

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IDH mutations occur in approximately 80% of low-grade gliomas, promoting tumorigenesis through increased levels of the oncometabolite D-2-hydroxyglutarate (2-HG). Data from the ongoing perioperative study found that treatment with vorasidenib 50 mg and TIBSOVO 500 mg resulted in mean percent reduction in 2-HG (95% CI) of 92.6% (76.1, 97.6) and 91.1% (72.0, 97.0), respectively, relative to untreated samples in patients with low-grade glioma.

"The updated data demonstrate that robust 2-HG suppression by vorasidenib and TIBSOVO resulted in positive changes in both the tumor cells and the tumor immune microenvironment," said Ingo Mellinghoff, M.D., Memorial Sloan Kettering Cancer Center, an investigator for the study. "These findings underscore that the mutant IDH enzyme plays an active role in the growth of low-grade gliomas and that IDH inhibition may play a significant role in the future treatment of these tumors."

The study data demonstrated that short-term treatment with vorasidenib and TIBSOVO reduced tumor cell proliferation, altered the epigenetic state, and promoted the expression of genes associated with cellular differentiation. Additionally, the data showed that treatment with vorasidenib and TIBSOVO activated interferon signaling and increased T-cell infiltration.

"These early results further support the role of IDH inhibition in treating patients with hard-to-treat cancers, including IDH mutant low-grade glioma," said Susan Pandya, M.D., Vice President, Clinical Development, Head of Cancer Metabolism Global Development, Servier Pharmaceuticals. "These data build on evidence that vorasidenib demonstrates anti-tumor activity through 2-HG suppression and we look forward to confirming the clinical benefit of vorasidenib in patients with IDH mutant low-grade gliomas in the global Phase 3 INDIGO study."

TIBSOVO (ivosidenib tablets) is currently approved in the U.S. as monotherapy for the treatment of adults with IDH1-mutant relapsed or refractory acute myeloid leukemia (AML) and for adults with newly diagnosed IDH1-mutant AML who are ≥75 years old or who have comorbidities that preclude the use of intensive induction chemotherapy.

Vorasidenib, an investigational, oral, brain-penetrant dual inhibitor of mutant IDH1 and IDH2 enzymes, is currently being evaluated in the registration-enabling Phase 3 INDIGO study as a potential treatment for patients with residual or recurrent grade 2 glioma.

Perioperative Study of Vorasidenib and TIBSOVO

Vorasidenib and TIBSOVO are being evaluated as a single agent in an ongoing perioperative study in IDH1-mutant Grade 2/3 glioma. The primary endpoint is 2-hydroxyglutarate (2-HG) concentration in tumors resected following presurgical treatment with vorasidenib and TIBSOVO compared with untreated control tumors. Patients were randomized to 500 mg TIBSOVO once daily, 50 mg vorasidenib once daily or the control arm in cohort 1; and 250 mg TIBSOVO twice daily or 10 mg vorasidenib once daily in cohort 2. Patients were treated for four weeks prior to surgery and had the option to continue postoperative treatment until disease progression.

About Glioma

Glioma presents in varying degrees of tumor aggressiveness, ranging from slower growing (low-grade glioma) to rapidly progressing (high-grade glioma-Glioblastoma Multiforme). Tumor enhancement is an imaging characteristic assessed by magnetic resonance imaging (MRI), and enhancing tumors are more likely to be high-grade.

Common symptoms of glioma include seizures, memory disturbance, sensory impairment and neurologic deficits. The long-term prognosis is poor, and regardless of treatment, the majority of patients with low-grade gliomas will have recurrent disease that will progress over time. Approximately 11,000 low-grade glioma patients are diagnosed annually in the U.S. and EU and somatic mutations in IDH1 and IDH2 occur in approximately 80% of low-grade gliomas.

Nektar Therapeutics to Participate in Fireside Chat at the Goldman Sachs 42nd Annual Global Healthcare Conference

On June 7, 2021 Nektar Therapeutics’ (Nasdaq: NKTR) senior management reported to participate in a virtual fireside chat at the upcoming Goldman Sachs 42nd Annual Global Healthcare Conference on Tuesday, June 8, 2021 at 2:10 p.m. Eastern Time (Press release, Nektar Therapeutics, JUN 7, 2021, View Source [SID1234583684]).

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The presentation will be accessible via a webcast through a link posted on the Investor Events section of the Nektar website: View Source This Webcast will be available for replay until July 9, 2021.