Olaparib

Global $6.7 Bn Ovarian Cancer Opportunity Analysis and Forecasts to 2028 - ResearchAndMarkets.com

Retrieved on: 
Tuesday, November 5, 2019

The "Ovarian Cancer: Opportunity Analysis and Forecasts to 2028" report has been added to ResearchAndMarkets.com's offering.

Key Points: 
  • The "Ovarian Cancer: Opportunity Analysis and Forecasts to 2028" report has been added to ResearchAndMarkets.com's offering.
  • The dramatic growth in the ovarian cancer market is largely attributed to the label expansions for PARP inhibitors such as Lynparza, Zejula and Rubraca.
  • In 2028, three PARP inhibitor drugs are expected to have combined revenue of $2.8bn, constituting more than 40% of the global ovarian cancer market.
  • Analysis of the current and future market competition in the global ovarian cancer market.

Growth of PARP (Poly ADP-ribose Polymerase) Inhibitors Market to be Impacted by Expanded Application of PARP Inhibitors | Technavio

Retrieved on: 
Friday, October 18, 2019

PARP (Poly ADP-ribose Polymerase) Inhibitors Market Landscape 2019-2023: Geographic landscape

Key Points: 
  • PARP (Poly ADP-ribose Polymerase) Inhibitors Market Landscape 2019-2023: Geographic landscape
    PARP (Poly ADP-ribose Polymerase) Inhibitors Market Landscape 2019-2023: Indication
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  • PARP inhibitors are known for their high efficacy in the treatment of diseases such as solid tumors.
  • Vendors save on R&D costs by incorporating single molecule of these inhibitors for conducting multiple pre-clinical and clinical trial studies.
  • The vast application landscape of PARP inhibitors encourages vendors to carry out research activities for new cancer indications.

Synthetic Lethality-based Drugs and Targets Market, 2019-2030

Retrieved on: 
Tuesday, October 1, 2019

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Key Points: 
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    Currently, there are four approved (and marketed) poly-ADP ribose polymerase (PARP) inhibitor drugs, which have been shown to operate based on the concept of synthetic lethality.
  • Further, several such drugs are being investigated for the treatment of a myriad of advanced oncological and non-oncological indications.
  • The 'Synthetic Lethality-based Drugs and Targets Market, 2019-2030: Focus on DNA Repair (including PARP Inhibitors) and Other Novel Cellular Pathways' report features an extensive study of the current market landscape and the future potential of the synthetic lethality-based therapeutics.
  • Further, it highlights the long-term opportunities (for drug developers) associated with individual targets, based on their popularity across different portals.

Synthetic Lethality-based Drugs and Targets Market, 2030

Retrieved on: 
Monday, September 30, 2019

DUBLIN, Sept. 30, 2019 /PRNewswire/ -- The "Synthetic Lethality-based Drugs and Targets Market, 2019-2030: Focus on DNA Repair (including PARP Inhibitors) and Other Novel Cellular Pathways" report has been added to ResearchAndMarkets.com's offering.

Key Points: 
  • DUBLIN, Sept. 30, 2019 /PRNewswire/ -- The "Synthetic Lethality-based Drugs and Targets Market, 2019-2030: Focus on DNA Repair (including PARP Inhibitors) and Other Novel Cellular Pathways" report has been added to ResearchAndMarkets.com's offering.
  • The Synthetic Lethality-based Drugs and Targets Market, 2019-2030: Focus on DNA Repair (including PARP Inhibitors) and Other Novel Cellular Pathways' report features an extensive study of the current market landscape and the future potential of the synthetic lethality-based therapeutics.
  • Currently, there are four approved (and marketed) poly-ADP ribose polymerase (PARP) inhibitor drugs, which have been shown to operate based on the concept of synthetic lethality.
  • One of the key objectives of the report was to estimate the existing market size and identify the future opportunity for synthetic lethality-based drugs, over the next decade.

Global Synthetic Lethality-based Drugs and Targets Market Report 2019-2030: Focus on DNA Repair (including PARP Inhibitors) and Other Novel Cellular Pathways - ResearchAndMarkets.com

Retrieved on: 
Monday, September 30, 2019

The "Synthetic Lethality-based Drugs and Targets Market, 2019-2030: Focus on DNA Repair (including PARP Inhibitors) and Other Novel Cellular Pathways" report has been added to ResearchAndMarkets.com's offering.

Key Points: 
  • The "Synthetic Lethality-based Drugs and Targets Market, 2019-2030: Focus on DNA Repair (including PARP Inhibitors) and Other Novel Cellular Pathways" report has been added to ResearchAndMarkets.com's offering.
  • The Synthetic Lethality-based Drugs and Targets Market, 2019-2030: Focus on DNA Repair (including PARP Inhibitors) and Other Novel Cellular Pathways' report features an extensive study of the current market landscape and the future potential of the synthetic lethality-based therapeutics.
  • Currently, there are four approved (and marketed) poly-ADP ribose polymerase (PARP) inhibitor drugs, which have been shown to operate based on the concept of synthetic lethality.
  • Further, several such drugs are being investigated for the treatment of a myriad of advanced oncological and non-oncological indications.

LYNPARZA (olaparib) Improved the Time Women Lived Without Disease Progression to 22 Months in the Broad Population and 37 Months in HRD-positive Patients as 1st-line Maintenance Treatment with Bevacizumab for Newly Diagnosed Advanced Ovarian Cancer

Retrieved on: 
Saturday, September 28, 2019

Overall Grade 3 or above adverse events (AEs) were 57% for LYNPARZA added to bevacizumab and 51% for bevacizumab alone.

Key Points: 
  • Overall Grade 3 or above adverse events (AEs) were 57% for LYNPARZA added to bevacizumab and 51% for bevacizumab alone.
  • AEs led to dose interruption in 54% of patients on LYNPARZA while 20% of patients discontinued treatment.
  • LYNPARZA is currently approved as 1st-line maintenance treatment in women with somatic and germline BRCA-mutated advanced ovarian cancer following response to platinum-based chemotherapy.
  • For 1st-line maintenance in advanced ovarian cancer and the metastatic breast cancer setting, physicians should select patients for therapy based on an FDA-approved companion diagnostic.

LYNPARZA® (olaparib) Phase 3 PAOLA-1 Trial Significantly Increased Progression-Free Survival as First-Line Maintenance Treatment with Bevacizumab for Newly-Diagnosed Advanced Ovarian Cancer

Retrieved on: 
Saturday, September 28, 2019

Overall Grade 3 or above (AEs) were 57% for LYNPARZA added to bevacizumab and 51% for bevacizumab alone.

Key Points: 
  • Overall Grade 3 or above (AEs) were 57% for LYNPARZA added to bevacizumab and 51% for bevacizumab alone.
  • It is approved in the U.S. as first-line maintenance treatment in BRCAm advanced ovarian cancer following response to platinum-based chemotherapy.
  • LYNPARZA is the only PARP inhibitor with positive Phase 3 trials in four different cancer types.
  • Ovarian cancer the eighth most common cause of death from cancer in women worldwide, with a five-year survival rate of approximately 19%.

Cyclacel Pharmaceuticals Announces First Patient Treated With Oral CYC065 in a Phase 1 Study in Patients With Advanced Solid Tumors

Retrieved on: 
Monday, September 9, 2019

We are excited to report that the first patient has been treated with oral CYC065 in part 3 of our Phase 1 study, said Spiro Rombotis, President and Chief Executive Officer of Cyclacel.

Key Points: 
  • We are excited to report that the first patient has been treated with oral CYC065 in part 3 of our Phase 1 study, said Spiro Rombotis, President and Chief Executive Officer of Cyclacel.
  • We look forward to reporting data from Part 2 and 3 of this study in 2020.
  • The DNA damage response program is evaluating an oral combination regimen of sapacitabine and venetoclax in patients with relapsed or refractory AML/MDS.
  • An IST is evaluating an oral combination regimen of sapacitabine and olaparib in patients with BRCA mutant breast cancer.

LYNPARZA® (olaparib) Phase 3 PAOLA-1 Trial Met Primary Endpoint as First-Line Maintenance Treatment with Bevacizumab for Advanced Ovarian Cancer

Retrieved on: 
Wednesday, August 14, 2019

The trial, in the first-line maintenance setting, compared LYNPARZA added to standard-of-care bevacizumab versus bevacizumab alone in women with or without BRCA-gene mutations.

Key Points: 
  • The trial, in the first-line maintenance setting, compared LYNPARZA added to standard-of-care bevacizumab versus bevacizumab alone in women with or without BRCA-gene mutations.
  • PAOLA-1 is the second positive Phase 3 trial with LYNPARZA in first-line advanced ovarian cancer.
  • Following positive results from the SOLO-1 trial for women with a BRCA gene mutation, the PAOLA-1 trial marks yet another positive Phase 3 trial for LYNPARZA as a first-line maintenance treatment for women with advanced ovarian cancer.
  • In this co-operative group trial sponsored by ARCAGY Research, maintenance treatment with LYNPARZA when added to a standard-of-care treatment was evaluated in an environment representative of real clinical practice.

LYNPARZA® (olaparib) Phase III Paola-1 Trial Met Primary Endpoint as 1st-line Maintenance Treatment With Bevacizumab for Advanced Ovarian Cancer

Retrieved on: 
Wednesday, August 14, 2019

PAOLA-1 is the second positive Phase III trial with LYNPARZA in 1st-line advanced ovarian cancer.

Key Points: 
  • PAOLA-1 is the second positive Phase III trial with LYNPARZA in 1st-line advanced ovarian cancer.
  • Following positive results from the SOLO-1 trial for women with a BRCA gene mutation, the PAOLA-1 trial marks yet another positive Phase III trial for LYNPARZA as a 1st-line maintenance treatment for women with advanced ovarian cancer.
  • LYNPARZA is currently approved as first-line maintenance treatment in BRCAm advanced ovarian cancer following response to platinum-based chemotherapy.
  • It is also approved for the maintenance treatment of platinum-sensitive relapsed ovarian cancer regardless of BRCA status.