Sangamo Therapeutics Announces Participation at Upcoming Investor Conferences

On August 30, 2019 Sangamo Therapeutics, Inc. (Nasdaq: SGMO), a genomic medicine company, announced today that management will present at the following investor conferences in September (Press release, Sangamo Therapeutics, AUG 30, 2019, View Source [SID1234539148]):

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Wells Fargo 2019 Healthcare Conference
Presentation Date: Thursday, Sept 5th at 10:55 a.m. Eastern Time
Location: Boston, MA
Morgan Stanley 17th Annual Global Healthcare Conference
Presentation Date: Monday, Sept 9th at 8:10 a.m. Eastern Time
Location: New York, NY
Presentations will be webcast live and may be accessed via a link on the Sangamo Therapeutics website in the Investors and Media section under Events and Presentations. The presentation will also be available on the Sangamo website after the event.

Oncology Venture publishes Interim Report for the period January – June 2019

On August 30, 2019 Oncology Venture A/S (OV:ST) ("Oncology Venture") reported the Interim Report for the period January – June 2019 (Press release, Oncology Venture, AUG 30, 2019, View Source [SID1234539147]). The report is available as an attached document and on the company’s website (www.oncologyventure.com).

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Comment from CEO Peter Buhl Jensen
"We have a rich pipeline of seven mature drug candidates, and data that show us which projects are closest to the next value inflection points. Our priorities now are to continue planning the pivotal study of LiPlaCis to compile the marketing application for dovitinib and its DRP and to prepare a pivotal study that can be the base for marketing authorization of ixabepilone".

Summary of the Half Year Report

Consolidated group revenue amounted to 0.5 MDKK (1.6 MDKK).
Consolidated group loss before depreciation amounted to -28.1 MDKK (-6.4 MDKK).
Consolidated group loss before net financials amounted to -28.6 MDKK (-6.4 MDKK).
Consolidated net result amounted to -36.9 MDKK (3.6 MDKK).
Consolidated earnings per share (EPS) amounted to -0.65 DKK (0.15 DKK).
2019 numbers reflect the merged entity and 2018 numbers (in brackets) reflect Medical Prognosis Institute A/S only.

Highlights during Q2 2019

On June 24, Oncology Venture announced that the European Patent Office will grant Oncology Venture a patent on LiPlaCis DRP, which covers 205 genes and predicts the response in individual patients based on a pre-treatment biopsy.

On June 13, Oncology Venture acquired an additional 8% ownership in the dovitinib project from Sass & Larsen ApS at a purchase price of DKK 5.4 million. Following the transaction, Oncology Venture’s ownership amounts to 63%. Further, Oncology Venture has negotiated an option to acquire Sass & Larsen’s remaining ownership in dovitinib at a price of DKK 0.7 million per percent of the ownership. The current deal replaces a previous deal which allowed Oncology Venture to obtain 85% ownership. There is currently no time limit to this option.

On June 4, it was announced that an e-abstract has been published in Journal of Clinical Oncology – an ASCO (Free ASCO Whitepaper) Journal –, describing that DRP (Drug Response Prediction) is able to predict which breast cancer patients will be high likelihood responders to neoadjuvant (before surgery) treatment with doxorubicin.

On June 3, Oncology Venture announced that the US FDA had provided its initial response to the IND application and proposed pivotal Phase 3 study of LiPlaCis in the US. The FDA has requested some additional testing of LiPlaCis related to the product characterization. Oncology Venture expects to have these additional tests completed in good time before initiation of the study. The study design will be adapted to accommodate FDA’s recommendation for the pivotal study.

On May 16, Oncology Venture confirmed that its rights issue had been successfully executed, raising a gross amount of approximately DKK 56 million. None of the commitments from guarantors were utilized. The capital increase is a result of DKK 48.7 million paid in cash and DKK 7.7 as a debt conversion. In the event that the investor warrants allocated to the new shares issued are exercised in full during the 12-month exercise period, the company expects to receive additional net proceeds from the offering of approximately DKK 105 million.

On May 5, it was announced that members of Oncology Venture’s management team had decided to participate in the rights issue.

On April 30, Oncology Venture provided news on DRP based analyses of biopsies from clinical trials with dovitinib. In addition to renal, endometrial and GIST tumors, Oncology Venture has now also shown in two new indications – liver cancer and breast cancer – that DRP can predict the responding patients. Moreover, it was announced that the first patient has been dosed with 2X-121 (PARPi) at the Dana Farber Cancer Institute, Boston, US for the treatment of advanced ovarian cancer. Also, Oncology Venture disclosed that it had submitted an Investigational New Drug Application for LiPlaCis and its DRP to the FDA, with the intention to start a pivotal study in metastatic breast cancer.

On April 10, a supplement to the rights issue prospectus from April 5, 2019 was published. The reason for the supplement was that the company had obtained additional subscription undertakings from investors, raising the total undertaking to (DKK 56 million), and that the exercise periods for the Investor Warrants had been extended. Finally, a correction had been made in the terms for the Investor Warrants with regards to the exercise price.

On April 5, the Board of Directors of Oncology Venture decided to conduct a rights issue of shares supported by an authorization granted at the Annual General Meeting on April 4, 2019. The rights issue comprised of up to 25,155,639 offer units, each consisting of one new share at a subscription price of SEK 4/DKK 2.87 and one warrant at an exercise price of SEK 7.50.

On April 4, the Company announced that it has obtained an exclusive option to in-license the European rights to IXEMPRA (ixabepilone) from the pharmaceutical company R-Pharm U.S., LLC. In July 2015, R-PHARM U.S., LLC acquired global rights to IXEMPRA from Bristol-Myers Squibb (BMS). The drug is approved in the USA for the treatment of breast cancer. Oncology Venture will evaluate ixabepilone together with its drug specific DRP companion diagnostic in order to accomplish a market approval in Europe.

On April 3, it was announced that Oncology Venture intends to submit a new drug application to the FDA for marketing approval of dovitinib based on existing Novartis data in renal cancer. Also, the development of a new combination biomarker – PD1 – PD-L1/Dovitinib DRP has been completed. This gives a strong competitive edge in the immuno-oncology field. Oncology Venture has appointed US based Destum Partners to support its out-licensing activities.

Highlights after the period

On August 15 Oncology Venture informed that the US Food & Drug administration (FDA) had approved an IDE (Investigational Device Exemption) application for use of the company’s drug response predictor LiPlaCis DRP in a planned pivotal Phase 3 study. And in parallel, the FDA is evaluating Oncology Venture’s IND (Investigational New Drug) application for the drug substance LiPlaCis, which is primarily being developed as a potential new treatment of metastatic breast cancer in heavily pre-treated patients.
For investor inquiries
Ulla Hald Buhl, IR & Communications
E-mail: [email protected]
Telephone +45 21 70 10 49

For media inquiries
Thomas Pedersen, Carrotize PR & Communications
E-mail: [email protected]
Telephone +45 60 62 93 90

Y-mAbs Announces Data to be Presented at 2019 CTOS

On August 30, 2019 Y-mAbs Therapeutics, Inc. (the "Company" or "Y-mAbs") (Nasdaq: YMAB) a late-stage clinical biopharmaceutical company focused on the development and commercialization of novel, antibody-based therapeutic products for the treatment of cancer, is reported the acceptance of abstracts for a poster presentation and an oral presentation at the 2019 Connective Tissue Oncology Society (CTOS) Annual Meeting held November 13 through November 16, 2019 in Tokyo, Japan (Press release, Y-mAbs Therapeutics, AUG 30, 2019, View Source [SID1234539145]).

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The abstracts include the following presentations of omburtamab, one of the Company’s lead product candidates, which is currently being evaluated for the treatment of patients with CNS/Leptomeningeal metastasis from neuroblastoma, diffuse intrinsic pontine glioma ("DIPG"), and desmoplastic small round cell tumors ("DSRCT"):

· "Intraperitoneal radioimmunotherapy for desmoplastic small round cell tumor: Final results of a phase I study (clinicaltrials.gov identifier NCT01099644)," submitted by Memorial Sloan Kettering Cancer Center (MSK) in New York (poster presentation)

· "Whole abdominopelvic radiotherapy and radioimmunotherapy after complete resection of desmoplastic small round cell tumor (DSRCT): Major impact on survival," submitted by MSK in New York (oral presentation)

Ultragenyx to Present at Upcoming Investor Conferences

On August 30, 2019 Ultragenyx Pharmaceutical Inc. (NASDAQ: RARE), a biopharmaceutical company focused on the development of novel products for serious rare and ultra-rare genetic diseases, reported that Shalini Sharp, the company’s Chief Financial Officer, will present at the following conferences (Press release, Ultragenyx Pharmaceutical, AUG 30, 2019, View Source [SID1234539144]):

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Baird Global Healthcare Conference on Thursday, September 5, 2019 at 12:50pm ET in New York, NY

Morgan Stanley 17TH Annual Global Healthcare Conference on Wednesday, September 11, 2019 at 2:10pm ET in New York, NY
The live and archived webcast of the company presentations will be accessible from the company’s website at View Source The replay of the webcast will be available for 90 days.

Chugai Files for Additional Indication for Anti-HER2 Antibody Drug Conjugate Kadcyla for Adjuvant Therapy of HER2-Positive Early Breast Cancer

On August 30, 2019 Chugai Pharmaceutical Co., Ltd. (TOKYO: 4519) reported that it has filed an application to the Ministry of Health, Labour and Welfare (MHLW) in Japan for an additional indication for anti-HER2 antibody-tubulin polymerization inhibitor conjugate Kadcyla (generic name: trastuzumab emtansine), as adjuvant therapy in patients with HER2-positive early breast cancer (Press release, Chugai, AUG 30, 2019, View Source [SID1234539143]).

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"There is still a high unmet medical need for the development of treatment methods when pathologic complete response (pCR) is not obtained by neoadjuvant therapy. This application is the first step in providing patients with Kadcyla as a new treatment option of adjuvant therapy," said Dr. Yasushi Ito, Chugai’s Executive Vice President, Co-Head of Project & Lifecycle Management Unit. "Our HER2 franchise, consisting of Herceptin, Perjeta and Kadcyla has contributed to improving the outcomes of HER2-positive breast cancer. In this indication, we will continue to discuss with the regulatory authorities for the early approval of Kadcyla."

This application is based on results from an open-label, randomized, global phase III clinical study (the KATHERINE study), evaluating efficacy and safety of Kadcyla adjuvant therapy compared to Herceptin in almost 1,500 people with HER2-positive early breast cancer who had invasive residual disease in the breast and/or axillary lymph nodes following neoadjuvant therapy including Herceptin. The primary endpoint of the study was invasive disease-free survival (IDFS) Based on the results of the study, the U.S. Food and Drug Administration (FDA) granted Breakthrough Therapy Designation to Kadcyla as adjuvant therapy and gave regulatory approval on May 3, 2019, which is just over 12 weeks after submission under the FDA’s Real-Time Oncology Review pilot program.

The main results from the KATHERINE study are as follows:
– According to the first interim analysis of the primary endpoint, the superiority of Kadcyla over Herceptin in IDFS has been confirmed (unstratified hazard ratio: 0.50 [95% confidence interval: 0.39-0.64, log-rank test, p<0.0001].
– No superiority of Kadcyla over Herceptin in overall survival was observed in the first interim analysis of the secondary endpoint conducted at the same time.
– Adverse events were observed in 731 patients (98.8%) in Kadcyla group, which was consistent with the safety profile of Kadcyla in patients with HER2-positive metastatic breast cancer. Kadcyla as an adjuvant therapy was also well tolerated in patients with HER2-positive early breast cancer.

As a leading company in the field of oncology, Chugai will work to obtain approval for the additional indication to further contribute to the treatment of HER2-positive breast cancer.

[Reference information]
Media release issued by Roche on May 6, 2019
Title: FDA approves Roche’s Kadcyla for adjuvant treatment of people with HER2-positive early breast cancer with residual invasive disease after neoadjuvant treatment
View Source