The Timing of Toxicological Studies to Support Clinical Trials
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Published By Springer Netherlands

9789401046237, 9789401114240

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Phase I clinical trials: what is the minimum preclinical package necessary for initiating single-dose studies in man? — a toxicologist’s opinion

The Timing of Toxicological Studies to Support Clinical Trials ◽

10.1007/978-94-011-1424-0_5 ◽

1994 ◽

pp. 53-60

Author(s):

Herman Van Cauteren

Keyword(s):

Clinical Trials ◽

Single Dose ◽

Phase I ◽

Phase I Clinical Trials

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Reproductive and developmental toxicity studies required to support the inclusion of women and children in clinical trials — a toxicologist’s opinion

The Timing of Toxicological Studies to Support Clinical Trials ◽

10.1007/978-94-011-1424-0_9 ◽

1994 ◽

pp. 85-93

Author(s):

Kurt Suter

Keyword(s):

Clinical Trials ◽

Developmental Toxicity ◽

Toxicity Studies ◽

Women And Children

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The duration of toxicity studies required to support repeated dosing in clinical investigation — a toxicologist’s opinion

The Timing of Toxicological Studies to Support Clinical Trials ◽

10.1007/978-94-011-1424-0_7 ◽

1994 ◽

pp. 67-74 ◽

Cited By ~ 4

Author(s):

Toshiji Igarashi

Keyword(s):

Clinical Investigation ◽

Toxicity Studies ◽

Repeated Dosing

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The timing of reproductive toxicity studies in relation to clinical trials

The Timing of Toxicological Studies to Support Clinical Trials ◽

10.1007/978-94-011-1424-0_12 ◽

1994 ◽

pp. 115-125 ◽

Cited By ~ 1

Author(s):

Jeanne M Manson ◽

Fritz R Bühler

Keyword(s):

Clinical Trials ◽

Reproductive Toxicity ◽

Toxicity Studies

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Review of international recommendations on animal toxicity studies and their relation to clinical exposure

The Timing of Toxicological Studies to Support Clinical Trials ◽

10.1007/978-94-011-1424-0_2 ◽

1994 ◽

pp. 17-25 ◽

Cited By ~ 1

Author(s):

David Scales ◽

Toshimi Usui

Keyword(s):

Clinical Exposure ◽

Toxicity Studies ◽

Animal Toxicity

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The minimum non-clinical package for initiating Phase I clinical trials

The Timing of Toxicological Studies to Support Clinical Trials ◽

10.1007/978-94-011-1424-0_10 ◽

1994 ◽

pp. 99-108

Author(s):

Michael R Jackson ◽

Jack H Dean

Keyword(s):

Clinical Trials ◽

Phase I ◽

Phase I Clinical Trials

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The duration of toxicity studies required to support repeated dosing in clinical investigation — a clinician’s opinion

The Timing of Toxicological Studies to Support Clinical Trials ◽

10.1007/978-94-011-1424-0_8 ◽

1994 ◽

pp. 75-83

Author(s):

Kurt Suter

Keyword(s):

Clinical Investigation ◽

Toxicity Studies ◽

Repeated Dosing

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Input to ICH

The Timing of Toxicological Studies to Support Clinical Trials ◽

10.1007/978-94-011-1424-0_14 ◽

1994 ◽

pp. 133-139

Author(s):

R Michael McClain

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Considerations for implementing a toxicity testing strategy

The Timing of Toxicological Studies to Support Clinical Trials ◽

10.1007/978-94-011-1424-0_4 ◽

1994 ◽

pp. 41-49

Author(s):

Douglas M Morton

Keyword(s):

Toxicity Testing ◽

Testing Strategy

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International survey on the timing of toxicity studies in relation to clinical trials

The Timing of Toxicological Studies to Support Clinical Trials ◽

10.1007/978-94-011-1424-0_3 ◽

1994 ◽

pp. 27-39 ◽

Cited By ~ 1

Author(s):

Christopher Parkinson

Keyword(s):

Clinical Trials ◽

International Survey ◽

Toxicity Studies

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The Timing of Toxicological Studies to Support Clinical TrialsLatest Publications

TOTAL DOCUMENTS

H-INDEX

Published By Springer Netherlands

Phase I clinical trials: what is the minimum preclinical package necessary for initiating single-dose studies in man? — a toxicologist’s opinion

Reproductive and developmental toxicity studies required to support the inclusion of women and children in clinical trials — a toxicologist’s opinion

The duration of toxicity studies required to support repeated dosing in clinical investigation — a toxicologist’s opinion

The timing of reproductive toxicity studies in relation to clinical trials

Review of international recommendations on animal toxicity studies and their relation to clinical exposure

The minimum non-clinical package for initiating Phase I clinical trials

The duration of toxicity studies required to support repeated dosing in clinical investigation — a clinician’s opinion

Input to ICH

Considerations for implementing a toxicity testing strategy

International survey on the timing of toxicity studies in relation to clinical trials

The Timing of Toxicological Studies to Support Clinical Trials
Latest Publications