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Anti-angiogenesis therapy for the treatment of ovarian cancer

A technology for ovarian cancer and therapy, applied in the direction of anti-growth factor immunoglobulin, antibody, anti-tumor drugs, etc., can solve the problem of high mortality rate of cases

Pending Publication Date: 2019-09-13
F HOFFMANN LA ROCHE & CO AG
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Despite advances in patient management, the disease still has a high death-to-case ratio for all obstetrical malignancies diagnosed in the United States

Method used

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  • Anti-angiogenesis therapy for the treatment of ovarian cancer
  • Anti-angiogenesis therapy for the treatment of ovarian cancer
  • Anti-angiogenesis therapy for the treatment of ovarian cancer

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0306] Example 1: Carboplatin and Paclitaxel plus Placebo vs. Carboplatin and Paclitaxel plus Concurrent Bevacizumab, followed by Placebo, Versus Carboplatin and Paclitaxel plus Concurrent and Extended Bevacizumab Anti, stage III in women with newly diagnosed, previously untreated, stage III (suboptimal and macroscopically optimal massively resected) or IV epithelial ovarian, primary peritoneal, or fallopian tube cancer test

[0307] Presents results from a phase III randomized study in patients with International Federation of Obstetrics and Gynecologic Oncology (FIGO) stages III and IV epithelial ovarian, primary peritoneal or fallopian tube cancer (epithelial ovarian, peritoneal primary or fallopian tube cancer). ) patients were evaluated for new treatment procedures. The primary objective included identifying the addition of five concurrent cycles of bevacizumab to six in women with newly diagnosed stage III (with any overall residual disease) and stage IV epithelial ovar...

Embodiment 2

[0361] Example 2. A randomized, two-arm, multicenter gynecologic cancer intergroup trial of adding bevacizumab to standard chemotherapy (carboplatin and paclitaxel) in patients with epithelial ovarian cancer

[0362] Results from a phase III randomized study (ICON7) to assess the safety and efficacy of adding bevacizumab to standard chemotherapy of carboplatin and paclitaxel are presented. The primary endpoint was determined in patients with newly diagnosed, histologically confirmed, high-risk International Federation of Gynecology and Obstetrics (FIGO) stages I and IIa (grade 3 or clear cell carcinoma only) and FIGO stages IIb-IV (all grades and All histologic types) epithelial ovarian, fallopian tube, or primary peritoneal carcinoma, who have undergone primary surgery (mass excisional cytoreductive surgery or biopsy if the patient has FIGO stage IV disease) and will not be diagnosed before disease progression Whether the addition of bevacizumab to standard chemotherapy impr...

Embodiment 3

[0453] Example 3. A phase III, multicenter, randomized, blinded, placebo-controlled trial of carboplatin and gemcitabine plus bevacizumab in patients with platinum-sensitive recurrent ovarian, primary peritoneal, or fallopian tube cancer

[0454] Epithelial ovarian carcinoma (EOC) and its histologic and clinical equivalents, primary peritoneal carcinoma (PPC) and fallopian tube carcinoma, occur in the United States at an incidence of approximately 25,000 cases per year and are responsible for approximately 14,000 deaths per year. Because the disease tends to be asymptomatic in its early stages, most patients initially present with advanced (stage III or IV) disease. Although EOC, PPC, and fallopian tube cancers are sensitive to multiple chemotherapeutic agents, especially taxanes and platinum compounds, only 20%>-30%>patients with stage III or IV disease will be alive at 5 years. Patients with platinum-sensitive recurrent cancer (defined as disease recurrence more than 6 mont...

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Abstract

The invention relates to an anti-angiogenesis therapy for the treatment of ovarian cancer. This invention concerns in general treatment of diseases and pathological conditions with anti-VEGF antibodies. More specifically, the invention concerns the treatment of human patients susceptible to or diagnosed with cancer using an anti-VEGF antibody, preferably in combination with one or more additionalanti-tumor therapeutic agents for the treatment of ovarian cancer.

Description

[0001] This application is a divisional application of an invention application with a filing date of February 22, 2011, a Chinese application number of 201180020417.9, and an invention title of "anti-angiogenesis therapy for the treatment of ovarian cancer". [0002] related application [0003] This application claims U.S. Provisional Application Serial No. 61 / 439,819 filed February 4, 2011; U.S. Provisional Application Serial No. 61 / 360,059 filed June 30, 2010; U.S. Provisional Application Serial No. filed June 3, 2010 61 / 351,231; and the priority and benefit of U.S. Provisional Application Serial No. 61 / 307,095, filed February 23, 2010, the specification of which is incorporated herein in its entirety. [0004] Material preservation [0005] The following hybridoma cell lines have been deposited with the American Type Culture Collection (ATCC), Manassas, VA, USA under the terms of the Budapest Treaty: [0006] [0007] field of invention [0008] In general, the presen...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61K39/395A61P35/00G06Q99/00A61K31/337A61K31/555
CPCA61K31/282A61K31/337G06Q99/00A61K39/39558C07K16/22A61K31/7068A61P15/00A61P35/00A61P43/00A61K2300/00C07K2317/56C07K16/3069C07K2317/24A61K2039/545A61K2039/54A61K9/0019A61K39/3955A61K45/06
Inventor J.杜邦C.伊尔
Owner F HOFFMANN LA ROCHE & CO AG