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1. Development of consensus-driven SPIRIT and CONSORT extensions for early phase dose-finding trials: the DEFINE study

2. Multi-outcome trials with a generalised number of efficacious outcomes

3. Two-stage single-arm trials are rarely reported adequately

5. Optimal curtailed designs for single arm phase II clinical trials

6. Bayesian Adaptive Designs for Phase I Trials

7. Blinded and unblinded sample size re-estimation in crossover trials balanced for period

8. Design optimisation and post-trial analysis in group sequential stepped-wedge cluster randomised trials

9. Efficient determination of optimised multi-arm multi-stage experimental designs with control of generalised error-rates

10. A two-stage Fisher exact test for multi-arm studies with binary outcome variables

11. Calculations involving the multivariate normal and multivariate t distributions with and without truncation

14. Admissible multi-arm stepped-wedge cluster randomized trial designs

15. Group Sequential Crossover Trial Designs with Strong Control of the Familywise Error Rate

16. An optimised multi-arm multi-stage clinical trial design for unknown variance

17. Group Sequential Clinical Trial Designs for Normally Distributed Outcome Variables

18. Blinded and unblinded sample size re-estimation procedures for stepped-wedge cluster randomized trials

19. C286, an orally available retinoic acid receptor β agonist drug, regulates multiple pathways to achieve spinal cord injury repair.

20. The Adaptive designs CONSORT Extension (ACE) statement : a checklist with explanation and elaboration guideline for reporting randomised trials that use an adaptive design

24. Phase 1 safety, tolerability, pharmacokinetics and pharmacodynamic results of KCL‐286, a novel retinoic acid receptor‐β agonist for treatment of spinal cord injury, in male healthy participants

26. Extended and standard duration weight-loss programme referrals for adults in primary care (WRAP): a randomised controlled trial

32. A stochastically curtailed single-arm phase II trial design for binary outcomes

37. Two-Stage Adaptive Designs for Three-Treatment Bioequivalence Studies

38. INNODIA Master Protocol for the evaluation of investigational medicinal products in children, adolescents and adults with newly diagnosed type 1 diabetes

39. INNODIA Master Protocol for the evaluation of investigational medicinal products in children, adolescents and adults with newly diagnosed type 1 diabetes

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