Bavarian Nordic Announces Updated Overall Survival Data from Combination Immunotherapy Data of PROSTVAC plus Ipilimumab at the 2015 Genitourinary Cancers Symposium

On February 24, 2015 Bavarian Nordic reported that updated overall survival data from an NCI sponsored combination study of Bavarian Nordic’s active prostate cancer immunotherapy candidate PROSTVAC and ipilimumab, an immune checkpoint inhibitor will be presented at the Genitourinary Cancers Symposium in Orlando, FL on Thursday, February 26, 2015 (Press release Bavarian Nordic, FEB 24, 2015, View Source [SID:1234501841]).

30 patients with metastatic castration-resistant prostate cancer (mCRPC) were enrolled in the Phase 1 combination study. At the time of enrollment docetaxel was the only FDA-approved treatment that improved overall survival. The median predicted overall survival (OS) was 18.5 months. Patients were treated with PROSTVAC plus escalating doses of ipilimumab. The observed median OS was 31.3 months for all dose cohorts and 37.2 months for patients treated at 10 mg/kg based on updated overall survival data. Furthermore, approximately 20% of patients at 10 mg/kg remain alive at 80 months.

The senior author for the presentation as a poster is Dr. James L. Gulley, Laboratory of Tumor Immunology and Biology, National Cancer Institute at the National Institutes of Health. The presentation will take place during General Poster Session A on Thursday, February 26, 2015 from 11:30 AM – 1:00 PM EST at board H8. An abstract entitled: “Combining active immunotherapy and immune checkpoint inhibitors in prostate cancer” (Abstract #172) is also available online at View Source

Paul Chaplin, President & CEO of Bavarian Nordic, said: “The updated long-term survival data presented by our partners at NCI is further evidence of improved OS following treatment with PROSTVAC. These data represent perhaps the most compelling survival benefit seen to date in this late-stage setting, and provide a strong rationale to continue to evaluate the combination of PROSTVAC and checkpoint inhibitors in follow-on clinical studies. Given the unique product profile of PROSTVAC, with a favorable risk-benefit profile and ease of use, we see PROSTVAC as an ideal immunotherapy to combine with both approved and emerging therapies for prostate cancer and we look forward to exploring these further in the clinic.”

10-K – Annual report [Section 13 and 15(d), not S-K Item 405]

PDL BioPharma has filed a 10-K – Annual report [Section 13 and 15(d), not S-K Item 405] with the U.S. Securities and Exchange Commission (Filing 10-K , PDL BioPharma, FEB 23, 2015, View Source [SID1234501849]).

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10-K – Annual report [Section 13 and 15(d), not S-K Item 405]

Ligand has filed a 10-K – Annual report [Section 13 and 15(d), not S-K Item 405] with the U.S. Securities and Exchange Commission (Filing 10-K , Ligand, FEB 23, 2015, View Source [SID1234501847]).

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10-Q – Quarterly report [Sections 13 or 15(d)]

Rich Pharmaceuticals has filed a 10-Q – Quarterly report [Sections 13 or 15(d)] with the U.S. Securities and Exchange Commission (Filing 10-Q , Rich Pharmaceuticals, FEB 23, 2015, View Source [SID1234501840]).

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Prescient Therapeutics Granted Key U.S. Patents for Novel Cancer Compound PTX-200

On February 23, 2015 Prescient Therapeutics (ASX: PTX), a clinical stage oncology company, announced today that the U.S Patent and Trademark Office has granted two additional patents that underpin the development and commercialisation of its drug candidate PTX-200. U.S. patent 8,906,869, provides broad protection for the company’s novel method of treating chemotherapy resistant ovarian cancer with the AKT inhibitorcompound PTX-200, formerly known as TCN-P or triciribine phosphate monohydrate (Press release, Prescient Therapeutics, FEB 23, 2015, View Source [SID1234517542]). The second U.S. patent 8,901,086, provides broad coverage for treating various cancer types including breast cancer by administering PTX-200 in combination with trastuzumab.

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Dr. Robert Crombie, Managing Director of Prescient Therapeutics, said, "These U.S. patents further enhance our intellectual property portfolio. They confirm our monopoly rights on this novel and highly encouraging compound which we believe has significant potential to improve the clinical outcome for women with chemotherapy-resistant ovarian cancer."

"Prescient’s drug candidate PTX-200 is being trialed in patients who have become resistant to platinum-based drugs as it inhibits the AKT tumor survival pathway associated with platinum drug resistance PTX-200, in combination with standard of care drug carboplatin, is currently in Phase 1b/2 trial as a new therapy for ovarian cancer, the fifth leading cause of cancer death in women in the United States. Currently approximately half of the patients diagnosed with ovarian cancer will die from metastatic disease as they become resistant to the platinum-based drugs that constitute front line therapy. Prescient’s drug candidate PTX-200 is aiming to minimise this resistance."