메뉴 건너뛰기




Volumn 23, Issue 4, 2002, Pages 367-379

An optimal two-stage phase II design utilizing complete and partial response information separately

Author keywords

Optimal; Phase II; Trinomial

Indexed keywords

ARTICLE; CANCER SURVIVAL; CLASSIFICATION; CLINICAL PRACTICE; COMPUTER PROGRAM; EXPERIMENTAL DESIGN; ONCOLOGY; PARAMETER; PHASE 2 CLINICAL TRIAL; PROBABILITY; SAMPLE SIZE; TREATMENT OUTCOME; TUMOR VOLUME;

EID: 0036344705     PISSN: 01972456     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0197-2456(02)00217-9     Document Type: Article
Times cited : (23)

References (19)
  • 1
    • 50549174560 scopus 로고
    • The determination of the number of patients required in a preliminary and a follow-up trial of a new chemotherapeutic agent
    • (1961) J Chronic Diseases , vol.13 , pp. 346-353
    • Gehan, E.A.1
  • 5
    • 0020108590 scopus 로고
    • One sample multiple testing procedure for phase II clinical trials
    • (1982) Biometrics , vol.38 , pp. 143-151
    • Fleming, T.R.1
  • 6
    • 0029591692 scopus 로고
    • Incorporating toxicity considerations into the design of two-stage phase II clinical trials
    • (1995) Biometrics , vol.51 , pp. 1372-1383
    • Bryant, J.1    Day, R.2
  • 9
    • 0030060408 scopus 로고    scopus 로고
    • New statistical strategy for monitoring safety and efficacy in single-arm clinical trials
    • (1996) J Clin Oncol , vol.14 , pp. 296-303
    • Thall, P.F.1    Simon, R.2
  • 12
  • 13
    • 0018596257 scopus 로고
    • Predictive probability early termination plans for phase II clinical trials
    • (1979) Biometrics , vol.35 , pp. 775-783
    • Herson, J.1
  • 14


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.