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Phase I Clinical Trial Designs: Bayesian Optimal Interval Design (BOIN) |  Precision For Medicine
Phase I Clinical Trial Designs: Bayesian Optimal Interval Design (BOIN) | Precision For Medicine

Recommended dosages in each arm. DLT, dose-limiting toxicity; RD,... |  Download Scientific Diagram
Recommended dosages in each arm. DLT, dose-limiting toxicity; RD,... | Download Scientific Diagram

Biostatistical intepretation series II Clinical Trials Phase I - mitigating  misinterpretation risk in dose escalation studies
Biostatistical intepretation series II Clinical Trials Phase I - mitigating misinterpretation risk in dose escalation studies

Adaptive design for identifying maximum tolerated dose early to accelerate  dose-finding trial | BMC Medical Research Methodology | Full Text
Adaptive design for identifying maximum tolerated dose early to accelerate dose-finding trial | BMC Medical Research Methodology | Full Text

A Multicenter Phase I/II Study of Obatoclax Mesylate Administered as a 3-  or 24-Hour Infusion in Older Patients with Previously Untreated Acute  Myeloid Leukemia | PLOS ONE
A Multicenter Phase I/II Study of Obatoclax Mesylate Administered as a 3- or 24-Hour Infusion in Older Patients with Previously Untreated Acute Myeloid Leukemia | PLOS ONE

Innovative design for a phase 1 trial with intra-patient dose escalation:  The Crotoxin study. - Abstract - Europe PMC
Innovative design for a phase 1 trial with intra-patient dose escalation: The Crotoxin study. - Abstract - Europe PMC

Multi-stage dose expansion cohort (MSDEC) design with Bayesian stopping rule
Multi-stage dose expansion cohort (MSDEC) design with Bayesian stopping rule

Study flow chart. DLT, dose-limiting toxicity. | Download Scientific Diagram
Study flow chart. DLT, dose-limiting toxicity. | Download Scientific Diagram

Frontiers | A Dose-Finding Trial for Hyperthermic Intraperitoneal Cisplatin  in Gynecological Cancer Patients Receiving Hyperthermic Intraperitoneal  Chemotherapy
Frontiers | A Dose-Finding Trial for Hyperthermic Intraperitoneal Cisplatin in Gynecological Cancer Patients Receiving Hyperthermic Intraperitoneal Chemotherapy

Flexibility of the BLRM in Dose-Escalation Trials
Flexibility of the BLRM in Dose-Escalation Trials

Outline
Outline

Bayesian Optimal Interval Design: A Simple and Well-Performing Design for  Phase I Oncology Trials. - Abstract - Europe PMC
Bayesian Optimal Interval Design: A Simple and Well-Performing Design for Phase I Oncology Trials. - Abstract - Europe PMC

Study protocol: phase 1 dose escalating study of Pressurized  Intra-Peritoneal Aerosol Chemotherapy (PIPAC) with oxaliplatin in  peritoneal metastasis
Study protocol: phase 1 dose escalating study of Pressurized Intra-Peritoneal Aerosol Chemotherapy (PIPAC) with oxaliplatin in peritoneal metastasis

Study design for dose-escalation cohorts and DLT rate (as calculated by...  | Download Scientific Diagram
Study design for dose-escalation cohorts and DLT rate (as calculated by... | Download Scientific Diagram

Innovative design for a phase 1 trial with intra-patient dose escalation:  The Crotoxin study - ScienceDirect
Innovative design for a phase 1 trial with intra-patient dose escalation: The Crotoxin study - ScienceDirect

Dose-Finding Schemes in Clinical Trials
Dose-Finding Schemes in Clinical Trials

Dose levels, enrollment, and DLT in days 1-42 | Download Table
Dose levels, enrollment, and DLT in days 1-42 | Download Table

Determining drug dose in the era of targeted therapies: playing it  (un)safe? | Blood Cancer Journal
Determining drug dose in the era of targeted therapies: playing it (un)safe? | Blood Cancer Journal

Dose-limiting toxicity (DLT) and maximum tolerated dose (MTD) in Phase... |  Download Table
Dose-limiting toxicity (DLT) and maximum tolerated dose (MTD) in Phase... | Download Table

On Biostatistics and Clinical Trials: Dose Limiting Toxicity (DLT) and  Common Toxicity Criteria (CTC) / Common Terminology Criteria for Adverse  Events (CTCAE)
On Biostatistics and Clinical Trials: Dose Limiting Toxicity (DLT) and Common Toxicity Criteria (CTC) / Common Terminology Criteria for Adverse Events (CTCAE)

Exposure driven dose escalation design with overdose control: Concept and  first real life experience in an oncology phase I trial - ScienceDirect
Exposure driven dose escalation design with overdose control: Concept and first real life experience in an oncology phase I trial - ScienceDirect

Designing phase I oncology dose escalation using dose–exposure–toxicity  models as a complementary approach to model‐based dose–toxicity models -  Pantoja - 2022 - CPT: Pharmacometrics & Systems Pharmacology - Wiley Online  Library
Designing phase I oncology dose escalation using dose–exposure–toxicity models as a complementary approach to model‐based dose–toxicity models - Pantoja - 2022 - CPT: Pharmacometrics & Systems Pharmacology - Wiley Online Library