OncoSec to Present at the Ladenburg Thalmann 2019 Healthcare Conference

On September 20, 2019 OncoSec Medical Incorporated (OncoSec) (NASDAQ: ONCS), a company developing late-stage intratumoral cancer immunotherapies, reported that Daniel J. O’Connor, President and Chief Executive Officer of OncoSec, will present a company overview at the Ladenburg Thalmann 2019 Healthcare Conference on Tuesday, September 24, 2019, at 3:30 p.m. Eastern Time in New York, NY (Press release, OncoSec Medical, SEP 20, 2019, View Sourcenews/detail/2007/oncosec-to-present-at-the-ladenburg-thalmann-2019-healthcare-conference" target="_blank" title="View Sourcenews/detail/2007/oncosec-to-present-at-the-ladenburg-thalmann-2019-healthcare-conference" rel="nofollow">View Source [SID1234539663]).

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A live audio webcast of the presentation will be available on the Investors section of OncoSec’s website at View Source, where it will be archived for approximately 30 days.

Astellas Receives Positive CHMP Opinion for XOSPATA® (gilteritinib) as a Monotherapy for Patients with Relapsed or Refractory Acute Myeloid Leukemia with a FLT3 Mutation

On September 20, 2019 Astellas Pharma Inc. (TSE: 4503, President and CEO: Kenji Yasukawa, Ph.D., "Astellas") reported that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted a positive opinion recommending the oral once-daily therapy XOSPATA (gilteritinib) as a monotherapy for the treatment of adult patients who have relapsed or refractory (resistant to treatment) acute myeloid leukemia (AML) with a FLT3 mutation (FLT3mut+) (Press release, Astellas, SEP 20, 2019, View Source [SID1234539662]).2 If approved by the European Commission (EC), gilteritinib has the potential to improve treatment outcomes for AML patients with the most common mutations – FLT3 internal tandem duplication (ITD) and FLT3 tyrosine kinase domain (TKD) – and would be one of the few advances for the treatment of AML in Europe over the past 40 years.1,3 Gilteritinib received accelerated assessment from the EMA, which allowed the CHMP to reduce the timeframe for approval.4

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"The data are encouraging, showing a significant improvement in overall survival (OS), and one-year survival rates doubled when comparing gilteritinib to the current standard of care," said Giovanni Martinelli, M.D., Institute of Hematology, S.Orsola-Malpighi University Hospital, Bologna, Italy, a study investigator. "For relapsed or refractory FLT3mut+ AML patients the current prognosis is poor, with median OS of less than six months following treatment with salvage chemotherapy. If approved by the EC, gilteritinib has the potential to change the treatment landscape."

The CHMP decision is based on results from the Phase 3 ADMIRAL trial, which investigated gilteritinib versus salvage chemotherapy in patients with relapsed or refractory FLT3mut+ AML.5 Patients treated with gilteritinib had significantly longer OS than those who received salvage chemotherapy.5 Median OS for patients who received gilteritinib was 9.3 months, compared to 5.6 months for patients who received salvage chemotherapy (Hazard Ratio = 0.64 (95% CI 0.49, 0.83), P=0.0004).5,6 Rates of one-year survival were 37% for patients who received gilteritinib, compared to 17% for patients who received salvage chemotherapy.5

"There is a high unmet need in AML and Astellas is committed to improving treatment options. Gilteritinib offers a potential new alternative for patients with relapsed or refractory FLT3mut+ AML, with data showing improved survival outcomes," said Andrew Krivoshik, M.D., Ph.D., Senior Vice President and Global Therapeutic Area Head, Oncology Development, Astellas. "Subject to EC approval, gilteritinib has the potential to provide new hope for clinicians, patients and their families."

The positive opinion from the CHMP will now be reviewed by the EC, which has the authority to approve medicines for the 28 European Union member countries, and is also valid in Iceland, Norway and Liechtenstein.7 In late 2018, gilteritinib was approved by regulatory agencies in the U.S. and Japan for the treatment of adult patients who have relapsed or refractory FLT3mut+ AML.8,9

About Gilteritinib
Gilteritinib was discovered through a research collaboration with Kotobuki Pharmaceutical Co., Ltd., and Astellas has exclusive global rights to develop, manufacture and commercialize gilteritinib. Last year gilteritinib received an Orphan Designation from the European Commission and received accelerated assessment from the EMA.4,10

In the U.S., gilteritinib was previously granted Orphan Drug Designation and Fast Track Designation by the Food and Drug Administration (FDA), and was approved in November 2018 for the treatment of adult patients with relapsed or refractory FLT3mut+ AML, based on interim complete remission/complete remission with partial hematologic recovery (CR/CRh) data from the Phase 3 ADMIRAL trial.8 Gilteritinib has also received approval for a supplemental New Drug Application (sNDA) from the FDA, adding Overall Survival (OS) data from the Phase 3 ADMIRAL trial in relapsed or refractory FLT3mut+ AML to the gilteritinib label.6 Full results from the ADMIRAL trial were presented at the American Association for Cancer Research (AACR) (Free AACR Whitepaper) Annual Meeting in April 2019.5

In Japan, gilteritinib received Orphan Drug Designation and SAKIGAKE Designation from the Japanese Ministry of Health, Labour and Welfare and was approved for the treatment of adult patients with relapsed or refractory FLT3mut+ AML in September 2018.9,11 In August 2019, the Japanese package insert for gilteritinib was revised to include information regarding OS data from the ADMIRAL trial.12

Astellas is currently investigating gilteritinib in various FLT3mut+ AML patient populations through several Phase 3 trials.

About the ADMIRAL Trial13
The Phase 3 ADMIRAL trial (NCT02421939) was an open-label, multicenter, randomized study of gilteritinib versus salvage chemotherapy in adult patients with FLT3mut+ who are refractory to or have relapsed after first-line AML therapy. The co-primary endpoints of the trial were OS and CR/CRh rates. The study enrolled 371 patients with relapsed or refractory AML and FLT3mut+ present in bone marrow or whole blood. Subjects were randomized in a 2:1 ratio to receive gilteritinib (120 mg5) or salvage chemotherapy.

The most common adverse events (AEs) across both treatment arms of the ADMIRAL trial were febrile neutropenia (43.7%), anemia (43.4%), and pyrexia (38.6%).5 Common grade ≥3 AEs related to gilteritinib were anemia (19.5%), febrile neutropenia (15.4%), thrombocytopenia (12.2%), and decreased platelet count (12.2%).5 Adjusted for exposure duration, serious treatment-emergent AEs per patient year were less common with gilteritinib (7.1%) than salvage chemotherapy (9.2%).5

Chugai Obtains Approval for Additional Indication and Formulation for Tecentriq in PD-L1-Positive Triple Negative Breast Cancer

On September 20, 2019 Chugai Pharmaceutical Co., Ltd. (TOKYO: 4519) reported that it has obtained regulatory approval for its humanized anti-PD-L1 monoclonal antibody, Tecentriq [generic name: atezolizumab (genetical recombination)] from the Ministry of Health, Labour and Welfare (MHLW) for an additional indication of PD-L1-positive, hormone receptor-negative and HER2-negative inoperable or metastatic breast cancer (Press release, Chugai, SEP 20, 2019, View Source [SID1234539661]). It has also obtained approval for an additional formulation of Tecentriq 840 mg. Tecentriq 840 mg was developed to provide an optimal formulation for breast cancer for which approved dosage is 840 mg once every 2 weeks.

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VENTANA OptiView PD-L1 (SP142), a pathological testing kit marketed by Roche Diagnostics K.K., should be used to detect PD-L1 expression. An expanded use of VENTANA OptiView PD-L1 (SP142) as a companion diagnostic of Tecentriq was approved on August 20, 2019 to allow physicians to identify patients with PD-L1-positive breast cancer who could benefit from Tecentriq.

"We are very pleased that Tecentriq has been approved as the first immune checkpoint inhibitor for the treatment of PD-L1-positive triple-negative breast cancer (TNBC) in Japan," said Dr. Yasushi Ito, Chugai’s Executive Vice President, Co-Head of Project & Lifecycle Management Unit. "This approval provides a novel cancer immunotherapy-based treatment for TNBC, a rapidly-progressing cancer with limited therapeutic options. We are committed to contribute to patients through the treatment."

This approval is based on the results from the phase III IMpassion130 study. Tecentriq in combination with nab-paclitaxel (albumin-bound) met primary endpoint with a significant reduction in the risk of disease worsening or death (PFS) compared with nab-paclitaxel (albumin-bound) alone in the intention-to-treat (ITT) population (median PFS=7.2 vs 5.5 months; hazard ratio [HR]=0.80, 95%CI: 0.69-0.92, p=0.0025) and in people who were tested positive for PD-L1 expression (median PFS=7.5 vs 5 months; hazard ratio [HR]=0.62, 95% CI: 0.49-0.78, p<0.0001). Tecentriq and nab-paclitaxel (albumin-bound) showed a clinically meaningful improvement in the co-primary endpoint of overall survival (OS) in the PD-L1-positive population (median OS=25.0 vs 18.0 months; HR=0.71, 95% CI: 0.54-0.93) at the second interim analysis. OS results in the PD-L1-positive population were not formally tested due to the hierarchical design of the study as statistical significance was not met for OS in the intention-to-treat (ITT) population (median OS=21.0 vs 18.7 months; HR=0.86, 95% CI: 0.72-1.02, p=0.078). Follow-up will continue until the next planned analysis. The safety profile of Tecentriq in combination with chemotherapy was consistent with the known safety profiles of the individual medicines, and no new safety signals were identified.

About the IMpassion130 study
The IMpassion130 study is a Phase III, multicenter, randomized, double-blind study evaluating the efficacy, safety and pharmacokinetics of Tecentriq plus nab-paclitaxel (albumin-bound) compared with nab-paclitaxel (albumin-bound) in people with unresectable locally advanced or metastatic TNBC who have not received prior systemic therapy for metastatic breast cancer. The co-primary endpoints are PFS per investigator assessment (RECIST 1.1) and OS in the ITT population and in the PD-L1-positive population.


Roche’s Tecentriq in combination with Abraxane improves outcomes as an initial treatment for people with PD-L1-positive metastatic triple-negative breast cancer (Press release issued by Roche on October 20, 2018)
View Source

Chugai Files for Additional Indication and Additional Formulation of Anti-PD-L1 Antibody TECENTRIQ for Breast Cancer (Press release issued by Chugai on December 21, 2018)
View Source

Roche presents data from across its breast cancer portfolio at the 2019 American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) Annual Meeting (Press release issued by Roche on June 3, 2019)
View Source

Free Offering of Tecentriq 840 mg prior to the Listing in the NHI Reimbursement Price List
Under the system for healthcare services provided combining insurance-covered and non-covered services provided by MHLW, Chugai will offer Tecentriq for free to respond to requests for emergency use from patients with PD-L1-positive, hormone receptor-negative and HER2-negative inoperable or metastatic breast cancer with very limited treatment options. In the context of proper use, Tecentriq will be offered for free only to medical institutions participated in the clinical study of IMpassion130 study for development of the drug as clinical sites on condition that; 1) they would use the drug in accordance with the approved indications and dosage and administration and 2) they would corporate with us in implementing various safety measures to promote proper use, including activities based on Early Post-Marketing Phase Vigilance conducted by Chugai during the free offering period. The offering will start immediately after the date of regulatory approval and end on the day before the listing in the NHI reimbursement price list.

Sites for implementation of free offering of the drug Medical institutions participated in the clinical study of IMpassion130 study in Japan
Period for implementation of free offering of the drug From date of regulatory approval through the day before the listing in the NHI reimbursement price list
As a top pharmaceutical company in the field of oncology in Japan, Chugai is committed to contribute to patients and medical professionals by offering Tecentriq as a new treatment option and accordingly, to improve access of medications and their proper use.

Prescribing Information *The underlined parts were newly added.

Product name Tecentriq Intravenous Infusion 840 mg
Tecentriq Intravenous Infusion 1200 mg
Generic name atezolizumab (genetical recombination)
Indications Tecentriq Intravenous Infusion 840 mg
PD-L1-positive, hormone receptor-negative and HER2-negative inoperable or metastatic breast cancer
Tecentriq Intravenous Infusion 1200 mg
Unresectable, advanced or recurrent non-small cell lung cancer
Extensive-stage small cell lung cancer
Dosage and administration
In case of patients with untreated unresectable, advanced or recurrent non squamous non-small cell lung cancer.
The usual adult is 1200 mg atezolizumab (genetical recombination) in combination with carboplatin, paclitaxel and bevacizumab (genetical recombination) by intravenous infusion over 60 minutes once every 3 weeks. If the initial infusion is well tolerated, subsequent infusions can be delivered over 30 minutes.
In case of patients with unresectable, advanced or recurrent non squamous non-small cell lung cancer who has undergone chemotherapy.
The usual adult dosage is 1200 mg atezolizumab (genetical recombination) administered by intravenous infusion over 60 minutes once every 3 weeks. If the initial infusion is well tolerated, subsequent infusions can be delivered over 30 minutes.
In case of patients with extensive-stage small cell lung cancer.
The usual adult dosage is 1200 mg atezolizumab (genetical recombination) in combination with carboplatin and etoposide by intravenous infusion over 60 minutes once every 3 weeks. If the initial infusion is well tolerated, subsequent infusions can be delivered over 30 minutes.
In case of patients with PD-L1-positive, hormone receptor-negative and HER2-negative inoperable or metastatic breast cancer.
The usual adult dosage is 840 mg atezolizumab (genetical recombination) in combination with nab-paclitaxel (albumin-bound) administered by intravenous infusion over 60 minutes once every 2 weeks. If the initial infusion is well tolerated, subsequent infusions can be delivered over 30 minutes.
Drug price Tecentriq Intravenous Infusion 840 mg Not listed in the NHI price list
Tecentriq Intravenous Infusion 1200 mg JPY 625,567/per vial
Conditions for approval
A risk management plan should be created and appropriately implemented.
In case of patients with unresectable, advanced or recurrent non squamous non-small cell lung cancer who has undergone chemotherapy.
Because the number of participants in Japanese clinical trials was very limited, post-marketing drug use surveillance of all patients receiving Tecentriq treatment should be conducted until data for a certain number of patients have been accumulated, in order to understand background information on people using Tecentriq as well as to collect safety and efficacy data on Tecentriq promptly, and take necessary measures for the appropriate use of Tecentriq.
About Triple-Negative Breast Cancer
In Japan, 86,500 women (2018 predicted value) are estimated to be afflicted with breast cancer each year. 14,800 women in Japan (2018 predicted value) die as a result of the disease. Triple-negative breast cancer accounts for 15% of all breast cancer cases and, is more common in women under the age of 50, compared with other forms of breast cancer. Triple-negative breast cancer is defined by the lack of expression of hormone receptors (estrogen and progesterone receptors) and the overexpression of human epidermal growth factor receptor 2 (HER2). In general, triple-negative breast cancer has a high tumor-proliferative capacity and shorter overall survival, compared with other forms of breast cancer.

About approval status of Tecentriq in Japan
Tecentriq was launched in April 2018 with an indication of unresectable, advanced or recurrent NSCLC, followed by an approval for the additional dosing for the treatment of untreated unresectable, advanced or recurrent NSCLC in December 2018. In addition, an approval of extensive-stage small cell lung cancer has been obtained in August 2019.

Trademarks used or mentioned in this release are protected by law.

Sources

Cancer Registry and Statistics. Cancer Information Service, National Cancer Center Japan from: View Source Accessed August, 2019
Abramson VG et al. Subtyping of triple-negative breast cancer: implications for therapy. Cancer. 2015;121(1):8-16. 3.
Cancer Center. Triple negative breast cancer risk factors. [Internet; cited 2018 May 24]. Available from: View Source Accessed October 2018.
Pal SK et al. Triple negative breast cancer: unmet medical needs. Breast Cancer Res Treat. 2011;125(3):627-636.
American Cancer Society. Breast Cancer Facts & Figures 2013-2014
Lehmann BD et al. Identification of human triple-negative breast cancer subtypes and preclinical models for selection of targeted therapies. J Clin Invest. 2011;121(7):2750-67.

Bristol-Myers Squibb to Hold Investor Webcast to Discuss ESMO Highlights

On September 20, 2019 Bristol-Myers Squibb Company (NYSE: BMY) reported that it will host a webcast on Saturday, September 28, 2019 at 7:30 p.m. CEST (1:30 p.m. EDT) to discuss data presented at the European Society of Medical Oncology (ESMO) (Free ESMO Whitepaper), in Barcelona, Spain (Press release, Bristol-Myers Squibb, SEP 20, 2019, View Source [SID1234539660]). Company executives will provide an overview of data presented at the meeting, with a focus on the company’s Immuno-Oncology portfolio, and address inquiries from investors and analysts.

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Investors and the general public are invited to listen to a live webcast at: investor.bms.com and are urged to register prior to the webcast. Materials related to the call will be available at the same website prior to the call.

Mexican Institute of Industrial Property Granted AskAt a Use Patent of EP4 Receptor Antagonist for the Treatment of Cancer

On September 20, 2019 AskAt reported that it received a notice of allowance dated August 13, 2019 from the Mexican Institute of Industrial Property (IMPI: Instituto Mexicano de la Propiedad Industrial) in connection with the Mexican Patent Application No. MX/a/2016/008394, a use patent of EP4 receptor antagonist for the treatment of cancer (Press release, AskAt, SEP 20, 2019, View Source [SID1234539659]).

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