Vertaile menetelmiä
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| Retrospektiivinen vaiheen II kliininen tutkimus× | Vaiheen I kliininen tutkimus× | |
|---|---|---|
| Tieteenala | Epidemiologia | Epidemiologia |
| Menetelmäperhe | Process / pipeline | Process / pipeline |
| Syntyvuosi≠ | 1980s–1990s (with growth in oncology retrospective analyses) | 1960s (formal regulatory framework established ~1963–1970s) |
| Kehittäjä≠ | Adapted from standard Phase II trial methodology; retrospective variant formalized in oncology practice | Regulatory and clinical pharmacology community; formalized in U.S. FDA IND regulations (1963) and ICH guidelines |
| Tyyppi≠ | Observational retrospective study | Interventional clinical study design |
| Alkuperäislähde≠ | Simon, R. (1989). Optimal two-stage designs for phase II clinical trials. Controlled Clinical Trials, 10(1), 1–10. DOI ↗ | Storer, B. E. (1989). Design and analysis of phase I clinical trials. Biometrics, 45(3), 925–937. DOI ↗ |
| Rinnakkaisnimet | retrospective Phase II study, historical Phase II analysis, retrospective efficacy study, Phase II retrospective analysis | Phase 1 trial, first-in-human study, FIH study, dose-escalation study |
| Liittyvät≠ | 5 | 6 |
| Tiivistelmä≠ | A retrospective Phase II clinical trial evaluates a treatment's preliminary efficacy and safety signals using existing archival data — medical records, registries, or electronic health records — rather than prospectively enrolling new patients. It mirrors the objectives of a standard Phase II trial (estimating response rate, tolerability, and early efficacy) but does so by looking backward at patients who have already received the intervention, making it faster and less costly than a prospective design. | A Phase I clinical trial is the first stage of human testing for a new drug, biologic, or intervention. Its primary objective is to evaluate safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) rather than therapeutic efficacy. Small cohorts of participants — typically healthy volunteers or patients with advanced disease — receive sequentially increasing doses to identify the maximum tolerated dose (MTD) and the dose-limiting toxicities (DLTs) that define the boundary for subsequent trials. |
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