Terminology
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| Biomedical Research and Regulation Work Group | Maturity Level : N/A | Standards Status : Informative |
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Definition for Code SystemResearchStudyPhase
<?xml version="1.0" encoding="UTF-8"?> <CodeSystem xmlns="http://hl7.org/fhir"> <id value="research-study-phase"/> <meta><lastUpdated value="2022-09-10T05:52:37.223+11:00"/> <profile value="http://hl7.org/fhir/StructureDefinition/shareablecodesystem"/> </meta> <text> <status value="generated"/> <div xmlns="http://www.w3.org/1999/xhtml">Codes for the stage in the progression of a therapy from initial experimental use in humans in clinical trials to post-market evaluation. This code system http://terminology.hl7.org/CodeSystem/research-study-phase defines the following codes:<p> This code system <code> http://terminology.hl7.org/CodeSystem/research-study-phase</code> defines the following codes: </p> <table class="codes"><tr><td style="white-space:nowrap"><b> Code</b></td><td><b> Display</b></td><td><b> Definition</b></td></tr><tr><td style="white-space:nowrap">n-a<a name="research-study-phase-n-a"> </a></td><td> N/A</td><td> Trials without phases (for example, studies of devices or behavioral interventions).</td></tr><tr><td style="white-space:nowrap">early-phase-1<a name="research-study-phase-early-phase-1"> </a></td><td> Early Phase 1</td>Designation for optional exploratory trials conducted in accordance with the United States Food and Drug Administration's (FDA) 2006 Guidance on Exploratory Investigational New Drug (IND) Studies. Formerly called Phase 0.<td> Designation for optional exploratory trials conducted in accordance with the United States Food and Drug Administration's (FDA) 2006 Guidance on Exploratory Investigational New Drug (IND) Studies. Formerly called Phase 0.</td> </tr><tr><td style="white-space:nowrap">phase-1<a name="research-study-phase-phase-1"> </a></td><td> Phase 1</td>Includes initial studies to determine the metabolism and pharmacologic actions of drugs in humans, the side effects associated with increasing doses, and to gain early evidence of effectiveness; may include healthy participants and/or patients.<td> Includes initial studies to determine the metabolism and pharmacologic actions of drugs in humans, the side effects associated with increasing doses, and to gain early evidence of effectiveness; may include healthy participants and/or patients.</td> </tr><tr><td style="white-space:nowrap">phase-1-phase-2<a name="research-study-phase-phase-1-phase-2"> </a></td><td> Phase 1/Phase 2</td><td> Trials that are a combination of phases 1 and 2.</td></tr><tr><td style="white-space:nowrap">phase-2<a name="research-study-phase-phase-2"> </a></td><td> Phase 2</td>Includes controlled clinical studies conducted to evaluate the effectiveness of the drug for a particular indication or indications in participants with the disease or condition under study and to determine the common short-term side effects and risks.<td> Includes controlled clinical studies conducted to evaluate the effectiveness of the drug for a particular indication or indications in participants with the disease or condition under study and to determine the common short-term side effects and risks.</td> </tr><tr><td style="white-space:nowrap">phase-2-phase-3<a name="research-study-phase-phase-2-phase-3"> </a></td><td> Phase 2/Phase 3</td><td> Trials that are a combination of phases 2 and 3.</td></tr><tr><td style="white-space:nowrap">phase-3<a name="research-study-phase-phase-3"> </a></td><td> Phase 3</td>Includes trials conducted after preliminary evidence suggesting effectiveness of the drug has been obtained, and are intended to gather additional information to evaluate the overall benefit-risk relationship of the drug.<td> Includes trials conducted after preliminary evidence suggesting effectiveness of the drug has been obtained, and are intended to gather additional information to evaluate the overall benefit-risk relationship of the drug.</td> </tr><tr><td style="white-space:nowrap">phase-4<a name="research-study-phase-phase-4"> </a></td><td> Phase 4</td>Studies of FDA-approved drugs to delineate additional information including the drug's risks, benefits, and optimal use.<td> Studies of FDA-approved drugs to delineate additional information including the drug's risks, benefits, and optimal use.</td> </tr></table></div> </text> <extension url="http://hl7.org/fhir/StructureDefinition/structuredefinition-wg"> <valueCode value="brr"/> </extension> <extension url="http://hl7.org/fhir/StructureDefinition/structuredefinition-standards-status"> <valueCode value="draft"/> </extension> <extension url="http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm"> <valueInteger value="1"/> </extension> <url value="http://terminology.hl7.org/CodeSystem/research-study-phase"/> <identifier> <system value="urn:ietf:rfc:3986"/> <value value="urn:oid:2.16.840.1.113883.4.642.4.1247"/> </identifier><version value="5.0.0-ballot"/> <name value="ResearchStudyPhase"/> <title value="ResearchStudyPhase"/> <status value="draft"/> <experimental value="false"/><date value="2020-12-28T16:55:11+11:00"/> <publisher value="HL7 (FHIR Project)"/> <contact> <telecom> <system value="url"/> <value value="http://hl7.org/fhir"/> </telecom> <telecom> <system value="email"/> <value value="fhir@lists.hl7.org"/> </telecom> </contact>Codes for the stage in the progression of a therapy from initial experimental use in humans in clinical trials to post-market evaluation.<description value="Codes for the stage in the progression of a therapy from initial experimental use in humans in clinical trials to post-market evaluation."/> <caseSensitive value="true"/> <valueSet value="http://hl7.org/fhir/ValueSet/research-study-phase"/> <content value="complete"/> <concept> <code value="n-a"/> <display value="N/A"/> <definition value="Trials without phases (for example, studies of devices or behavioral interventions)."/> </concept> <concept> <code value="early-phase-1"/> <display value="Early Phase 1"/>Designation for optional exploratory trials conducted in accordance with the United States Food and Drug Administration's (FDA) 2006 Guidance on Exploratory Investigational New Drug (IND) Studies. Formerly called Phase 0.<definition value="Designation for optional exploratory trials conducted in accordance with the United States Food and Drug Administration's (FDA) 2006 Guidance on Exploratory Investigational New Drug (IND) Studies. Formerly called Phase 0."/> </concept> <concept> <code value="phase-1"/> <display value="Phase 1"/>Includes initial studies to determine the metabolism and pharmacologic actions of drugs in humans, the side effects associated with increasing doses, and to gain early evidence of effectiveness; may include healthy participants and/or patients.<definition value="Includes initial studies to determine the metabolism and pharmacologic actions of drugs in humans, the side effects associated with increasing doses, and to gain early evidence of effectiveness; may include healthy participants and/or patients."/> </concept> <concept> <code value="phase-1-phase-2"/> <display value="Phase 1/Phase 2"/> <definition value="Trials that are a combination of phases 1 and 2."/> </concept> <concept> <code value="phase-2"/> <display value="Phase 2"/>Includes controlled clinical studies conducted to evaluate the effectiveness of the drug for a particular indication or indications in participants with the disease or condition under study and to determine the common short-term side effects and risks.<definition value="Includes controlled clinical studies conducted to evaluate the effectiveness of the drug for a particular indication or indications in participants with the disease or condition under study and to determine the common short-term side effects and risks."/> </concept> <concept> <code value="phase-2-phase-3"/> <display value="Phase 2/Phase 3"/> <definition value="Trials that are a combination of phases 2 and 3."/> </concept> <concept> <code value="phase-3"/> <display value="Phase 3"/>Includes trials conducted after preliminary evidence suggesting effectiveness of the drug has been obtained, and are intended to gather additional information to evaluate the overall benefit-risk relationship of the drug.<definition value="Includes trials conducted after preliminary evidence suggesting effectiveness of the drug has been obtained, and are intended to gather additional information to evaluate the overall benefit-risk relationship of the drug."/> </concept> <concept> <code value="phase-4"/> <display value="Phase 4"/>Studies of FDA-approved drugs to delineate additional information including the drug's risks, benefits, and optimal use.<definition value="Studies of FDA-approved drugs to delineate additional information including the drug's risks, benefits, and optimal use."/> </concept> </ CodeSystem >
Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.
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