(Q52061495)

English

Optimal continuous sequential boundaries for monitoring toxicity in clinical trials: a restricted search algorithm.

scientific article published in June 2001

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/11391689

Optimal continuous sequential boundaries for monitoring toxicity in clinical trials: a restricted search algorithm. (English)

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/11391689

author name string

Goldman AI

1

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/11391689

Hannan PJ

2

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/11391689

language of work or name

0 references

publication date

1 June 2001

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/11391689

Statistics in Medicine

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/11391689

20

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/11391689

11

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/11391689

1575-1589

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/11391689

Interim analyses for randomized clinical trials: the group sequential approach

1 reference

https://api.crossref.org/works/10.1002%2FSIM.713

21 January 2018

Continuous and group sequential conditional probability ratio tests for phase II clinical trials.

1 reference

https://api.crossref.org/works/10.1002%2FSIM.713

21 January 2018

Practical Bayesian guidelines for phase IIB clinical trials.

1 reference

https://api.crossref.org/works/10.1002%2FSIM.713

21 January 2018

Bayesian sequential monitoring designs for single-arm clinical trials with multiple outcomes.

1 reference

https://api.crossref.org/works/10.1002%2FSIM.713

21 January 2018

New statistical strategy for monitoring safety and efficacy in single-arm clinical trials.

1 reference

https://api.crossref.org/works/10.1002%2FSIM.713

21 January 2018

Issues in designing sequential stopping rules for monitoring side effects in clinical trials.

1 reference

https://api.crossref.org/works/10.1002%2FSIM.713

21 January 2018

Incorporating toxicity considerations into the design of two-stage phase II clinical trials

1 reference

https://api.crossref.org/works/10.1002%2FSIM.713

21 January 2018

Identifiers

10.1002/SIM.713

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/11391689

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/11391689

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