CompletedNot Applicable

Post Marketing Surveillance Study To Observe Safety And Efficacy Of Eraxis® IV

South Korea244 participantsStarted 2012-03-02

Plain-language summary

The objective of this study is to collect the safety and efficacy data of Eraxis IV (anidulafungin) 100 mg according to Korea Ministry of Food and Drug Safety regulations.

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Exclusion criteria

. Retrospective Study Population 2.1. Inclusion Criteria

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Number of Participants With Treatment-Emergent Adverse Events (AEs) and Serious Adverse Events (SAEs)

Timeframe: From the time of first dosing of Eraxis until 28 calendar days after last dose of Eraxis

Number of Participants With Discontinuations From Study Treatment Due to Adverse Events (AEs)

Timeframe: From the time of first dosing of Eraxis until 28 calendar days after last dose of Eraxis

Duration of Adverse Events (AEs)

Timeframe: From the time of first dosing of Eraxis until 28 calendar days after last dose of Eraxis

Number of Adverse Events (AEs) by Severity

Timeframe: From the time of first dosing of Eraxis until 28 calendar days after last dose of Eraxis

Number of Participants With Outcome in Response to Adverse Events (AEs)

Timeframe: From the time of first dosing of Eraxis until 28 calendar days after last dose of Eraxis

Percentage of Treatment-Emergent Treatment-Related Adverse Events (AEs)

Timeframe: From the time of first dosing of Eraxis until 28 calendar days after last dose of Eraxis

Trial details

NCT IDNCT00802854

SponsorPfizer

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2016-05-20

Results submitted2017-05-17

View on ClinicalTrials.gov More Candidemia trials

What they're measuring

Number of Participants With Treatment-Emergent Adverse Events (AEs) and Serious Adverse Events (SAEs)

Timeframe: From the time of first dosing of Eraxis until 28 calendar days after last dose of Eraxis

Number of Participants With Discontinuations From Study Treatment Due to Adverse Events (AEs)

Timeframe: From the time of first dosing of Eraxis until 28 calendar days after last dose of Eraxis

Duration of Adverse Events (AEs)

Timeframe: From the time of first dosing of Eraxis until 28 calendar days after last dose of Eraxis

Number of Adverse Events (AEs) by Severity

Timeframe: From the time of first dosing of Eraxis until 28 calendar days after last dose of Eraxis

Number of Participants With Outcome in Response to Adverse Events (AEs)

Timeframe: From the time of first dosing of Eraxis until 28 calendar days after last dose of Eraxis

Percentage of Treatment-Emergent Treatment-Related Adverse Events (AEs)

Timeframe: From the time of first dosing of Eraxis until 28 calendar days after last dose of Eraxis