Can a cancer pill keep working outside the lab? a Real-World test begins
NCT ID NCT04553926
First seen Jul 23, 2026 · Last updated Jul 24, 2026 · Updated 1 time
Summary
This study monitors the safety and effectiveness of the drug olaparib (Lynparza) in people with ovarian, breast, prostate, or pancreatic cancer who are prescribed it as part of routine care in South Korea. Researchers will track side effects and how long the cancer stays under control without requiring extra study visits. The goal is to see how well the drug performs in everyday medical practice.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a PARP inhibitor drug called olaparib (Lynparza)
- What this could lead to
- If successful, this study could confirm that olaparib works safely in everyday clinical practice for several cancers.
- What could go wrong
- This is an observational post-marketing study, not a controlled trial, so it cannot prove cause and effect. Results may be influenced by how doctors choose treatments.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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661 people
The number who actually took part.
- Started
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Feb 2021
- Finished
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Jul 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
On active study drug treatment according to the approved local label.
- Ages
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19 to 150 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Eligible for the study drug treatment according to the approved label in South Korea 2. Provision of signed and dated written informed consent by the patient or legally acceptable representative Exclusion Criteria: 1. History of hypersensitivity to excipients of the study drug or to drugs with a similar chemical structure or class to the study drug 2. Prior exposure to any Polyadenosine 5'diphosphoribose polymerase (PARP) inhibitors, including the study drug 3. Pregnant and/or breast feeding 4. Current participation in any interventional trial 5. Other off-label indications according to the approved label
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Research Site
Ansan, South Korea
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Research Site
Bucheon-si, South Korea
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Research Site
Busan, South Korea
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Research Site
Changwon, South Korea
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Research Site
Daegu, South Korea
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Research Site
Daejeon, South Korea
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Research Site
Goyang, South Korea
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Research Site
Gunpo, South Korea
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Research Site
Hwaseong, South Korea
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Research Site
Ilsan, South Korea
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Research Site
Incheon, South Korea
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Research Site
Jeonju, South Korea
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Research Site
Seongnam, South Korea
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Research Site
Seoul, South Korea
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Research Site
Suwon, South Korea
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Research Site
Uijeongbu-si, South Korea
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Research Site
Yangsan, South Korea
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Research Site
Yongin, South Korea
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- RE-irradiation for isolated FOCal recurrence of prostate cancer with ultrahypofracted SBRT: the RE-FOCUS study - pushing the boundaries of precision and efficacy
- Operationalising multifactorial ovarian cancer risk assessment using the CanRisk tool versus standard practices.
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