-
1
-
-
0029793053
-
Workshop on phase I study design
-
Arbuck SG (1996) Workshop on Phase I study design. Ann Oncol 7: 567-573
-
(1996)
Ann Oncol
, vol.7
, pp. 567-573
-
-
Arbuck, S.G.1
-
2
-
-
0025318468
-
Pharmacokinetics of 2,5-diaziridinyl-3,6-bis(2-hydroxyethylamino) 1,4-benzoquinone (BZQ. NSC224070) during a phase I clinical trial
-
Betteridge RF, Bosanquet AG and Gilby ED (1990) Pharmacokinetics of 2,5-diaziridinyl-3,6-bis(2-hydroxyethylamino) 1,4-benzoquinone (BZQ. NSC224070) during a Phase I clinical trial. Eur J Cancer 26: 107-112
-
(1990)
Eur J Cancer
, vol.26
, pp. 107-112
-
-
Betteridge, R.F.1
Bosanquet, A.G.2
Gilby, E.D.3
-
3
-
-
0028908050
-
Revisions of general guidelines cur the preclinical toxicology of new cytotoxic anticancer agents in Europe
-
Burtles SS, Newell DR, Henrar REC and Connors TA (1995) Revisions of general guidelines Cur the preclinical toxicology of new cytotoxic anticancer agents in Europe. Eur J Cancer 31A: 408-410
-
(1995)
Eur J Cancer
, vol.31 A
, pp. 408-410
-
-
Burtles, S.S.1
Newell, D.R.2
Henrar, R.E.C.3
Connors, T.A.4
-
4
-
-
0025217061
-
A phase I and pharmacokinetic study of didox administered by 36 hour infusion
-
Cartmichael J, Cantwell BMJ, Mannix KA, Veale D, Elford HL, Blackie R, Kerr DJ, Kaye SB and Harris AI. (1990) A Phase I and pharmacokinetic study of didox administered by 36 hour infusion. Br J Cancer 61: 447-450
-
(1990)
Br J Cancer
, vol.61
, pp. 447-450
-
-
Cartmichael, J.1
Cantwell, B.M.J.2
Mannix, K.A.3
Veale, D.4
Elford, H.L.5
Blackie, R.6
Kerr, D.J.7
Kaye, S.B.8
Harris, A.I.9
-
6
-
-
0025360796
-
Pharmacologically guided phase I clinical trials based upon preclinical drug development
-
Collins JM, Grieshaber CK and Chabner BA (1990) Pharmacologically guided Phase I clinical trials based upon preclinical drug development. J Natl Cancer Inst 82; 1321-1326
-
(1990)
J Natl Cancer Inst
, vol.82
, pp. 1321-1326
-
-
Collins, J.M.1
Grieshaber, C.K.2
Chabner, B.A.3
-
7
-
-
0025353690
-
Responses and toxic deaths in phase I clinical trials
-
Decoster G, Stein G and Holdener EE (1990) Responses and toxic deaths in Phase I clinical trials. Ann Oncol 1: 175-181
-
(1990)
Ann Oncol
, vol.1
, pp. 175-181
-
-
Decoster, G.1
Stein, G.2
Holdener, E.E.3
-
8
-
-
14444267319
-
Regulatory considerations for preclinical development of anticancer drugs
-
DeGeorge JJ, Ahn C-H, Andrews PA, Brower ME, Giorgio DW, Goheer ME, Lee-Ham DY, McGuinn WD, Schmidt W, Sun CJ and Tripathi SC (1998) Regulatory considerations for preclinical development of anticancer drugs. Cancer Chemother Pharmacol 41: 173-185
-
(1998)
Cancer Chemother Pharmacol
, vol.41
, pp. 173-185
-
-
Degeorge, J.J.1
Ahn, C.-H.2
Andrews, P.A.3
Brower, M.E.4
Giorgio, D.W.5
Goheer, M.E.6
Lee-Ham, D.Y.7
McGuinn, W.D.8
Schmidt, W.9
Sun, C.J.10
Tripathi, S.C.11
-
9
-
-
0029841357
-
Phase I trial design: Are new methodologies being put into practise?
-
Dent SF and Eisenhauer FA (1996) Phase I trial design: are new methodologies being put into practise? Ann Oncol 7; 561-566
-
(1996)
Ann Oncol
, vol.7
, pp. 561-566
-
-
Dent, S.F.1
Eisenhauer, F.A.2
-
10
-
-
0023184783
-
Pharmacokinetically guided dose escalation in phase I clinical trials
-
EORTC Pharmacokinetics and Metabolism Group (1987) Pharmacokinetically guided dose escalation in Phase I clinical trials. Eur J Cancer 23: 1083-1087
-
(1987)
Eur J Cancer
, vol.23
, pp. 1083-1087
-
-
-
11
-
-
0022542911
-
Therapeutic response in phase I trials of antineoplastic agents
-
Estey E, Hoth D, Simon R, Marsoni S, Leyland-Jones B and Wittes R (1986) Therapeutic response in Phase I trials of antineoplastic agents. Cancer Treat Rep 70; 1105-1115
-
(1986)
Cancer Treat Rep
, vol.70
, pp. 1105-1115
-
-
Estey, E.1
Hoth, D.2
Simon, R.3
Marsoni, S.4
Leyland-Jones, B.5
Wittes, R.6
-
12
-
-
0026511154
-
Phase I trial of the anthrapyrazole CI-941: Prospective evaluation of pharmacologically guided dose-escalation
-
Foster BJ, Newell DR, Graham MA, Gumbrell LA, Jenns KE, Kaye SB and Calvert All (1992) Phase I trial of the anthrapyrazole CI-941: prospective evaluation of pharmacologically guided dose-escalation. Eur J Cancer 28: 463-469
-
(1992)
Eur J Cancer
, vol.28
, pp. 463-469
-
-
Foster, B.J.1
Newell, D.R.2
Graham, M.A.3
Gumbrell, L.A.4
Jenns, K.E.5
Kaye, S.B.6
Calvert, A.7
-
13
-
-
0027460210
-
Preclinical, phase I and pharmacokinetic studies with the dimethyl phenyltriazene CB10-277
-
Foster BJ, Newell DR, Carmichael J, Harris AL, Gumbrell LA, Jones M, Gogard PM and Calvert AH (1993a) Preclinical, Phase I and pharmacokinetic studies with the dimethyl phenyltriazene CB10-277. Br J Cancer 67: 362-368.
-
(1993)
Br J Cancer
, vol.67
, pp. 362-368
-
-
Foster, B.J.1
Newell, D.R.2
Carmichael, J.3
Harris, A.L.4
Gumbrell, L.A.5
Jones, M.6
Gogard, P.M.7
Calvert, A.H.8
-
14
-
-
0027416379
-
Phase I trial with pharmacokinetics of CB10-277 given by 24 hours continuous infusion
-
Foster BJ, Newell DR, Gumbrell LA, Jenns KE and Calvert AH (1993b) Phase I trial with pharmacokinetics of CB10-277 given by 24 hours continuous infusion. Br J Cancer 67: 369-373
-
(1993)
Br J Cancer
, vol.67
, pp. 369-373
-
-
Foster, B.J.1
Newell, D.R.2
Gumbrell, L.A.3
Jenns, K.E.4
Calvert, A.H.5
-
15
-
-
0013909023
-
Quantitative comparison of toxicity of anticancer agents in mouse, rat, hamster, dog, monkey and man
-
Freireich EJ, Gehan EA, Rall DP, Schmidt LH and Skipper HE (1966) Quantitative comparison of toxicity of anticancer agents in mouse, rat, hamster, dog, monkey and man. Cancer Chemother Rep 50: 219-244
-
(1966)
Cancer Chemother Rep
, vol.50
, pp. 219-244
-
-
Freireich, E.J.1
Gehan, E.A.2
Rall, D.P.3
Schmidt, L.H.4
Skipper, H.E.5
-
16
-
-
0016821405
-
Quantitative prediction of drug toxicity in humans from toxicology in small and large animals
-
Goldsmith MA, Slavik M and Carter SK (1975) Quantitative prediction of drug toxicity in humans from toxicology in small and large animals. Cancer Res 35: 1354-1364
-
(1975)
Cancer Res
, vol.35
, pp. 1354-1364
-
-
Goldsmith, M.A.1
Slavik, M.2
Carter, S.K.3
-
17
-
-
0022572075
-
Relationship of preclinical toxicology to findings in early clinical trials
-
Grieshaber CK and Marsoni S (1986) Relationship of preclinical toxicology to findings in early clinical trials. Cancer Treat Rep 70: 65-72
-
(1986)
Cancer Treat Rep
, vol.70
, pp. 65-72
-
-
Grieshaber, C.K.1
Marsoni, S.2
-
18
-
-
0015339772
-
Quantitative relationships between toxic doses of antitumour chemotherapeutic agents in animals and man
-
Homan ER (1972) Quantitative relationships between toxic doses of antitumour chemotherapeutic agents in animals and man. Cancer Chemother Rep Part 3 3: 13-19
-
(1972)
Cancer Chemother Rep Part
, vol.33
, pp. 13-19
-
-
Homan, E.R.1
-
19
-
-
0022879286
-
A toxicity and pharmacokinetic study in man of the hypoxic-cell radiosensitizer RSU-1069
-
Norwich A, Holliday SB, Deacon JM and Peckham MJ (1986) A toxicity and pharmacokinetic study in man of the hypoxic-cell radiosensitizer RSU-1069. Br J Radiol 59: 1238-1240
-
(1986)
Br J Radiol
, vol.59
, pp. 1238-1240
-
-
Norwich, A.1
Holliday, S.B.2
Deacon, J.M.3
Peckham, M.J.4
-
20
-
-
0029084804
-
A phase I trial of bryostalin 1 in patients with advanced malignancy using a 24 hour intravenous infusion
-
Jayson GC, Crowther D, Prendiville J, McGown AT, Scheid C, Stern P, Young R, Brenchley P, Thang J, Owens S and Peltit GR (1995) A Phase I trial of bryostalin 1 in patients with advanced malignancy using a 24 hour intravenous infusion. Br J Cancer 72: 461-468
-
(1995)
Br J Cancer
, vol.72
, pp. 461-468
-
-
Jayson, G.C.1
Crowther, D.2
Prendiville, J.3
McGown, A.T.4
Scheid, C.5
Stern, P.6
Young, R.7
Brenchley, P.8
Thang, J.9
Owens, S.10
Peltit, G.R.11
-
21
-
-
0031908511
-
Dose-limiting neurotoxicity in a phase I study of penelomedine (NSC 388720, CRC 88-04), a synthetic α-picoline derivative, administered intravenously
-
Jodrell DI, Bowman A, Stewart M, Dunlop N, French R, MacLellan A, Cummings J and Smyih JF (1998) Dose-limiting neurotoxicity in a Phase I study of penelomedine (NSC 388720, CRC 88-04), a synthetic α-picoline derivative, administered intravenously. Br J Cancer 77; 808-811
-
(1998)
Br J Cancer
, vol.77
, pp. 808-811
-
-
Jodrell, D.I.1
Bowman, A.2
Stewart, M.3
Dunlop, N.4
French, R.5
Maclellan, A.6
Cummings, J.7
Smyih, J.F.8
-
22
-
-
0025273434
-
General guidelines for the preclinical toxicology of new cytotoxic anticancer agents in Europe
-
Joint Steering Committee of the EORTC and CRC (1990) General guidelines for the preclinical toxicology of new cytotoxic anticancer agents in Europe. Eur J Cancer 26; 411-414
-
(1990)
Eur J Cancer
, vol.26
, pp. 411-414
-
-
-
23
-
-
0024452962
-
6-trimethylmelamine)
-
6-trimethylmelamine). Cancer Rev 49; 5475-5479
-
(1989)
Cancer Rev
, vol.49
, pp. 5475-5479
-
-
Judson, I.R.1
Calvert, A.H.2
Rutty, C.J.3
Abel, G.4
Gumbrell, L.A.5
Graham, M.A.6
Evans, B.D.7
Wilman, D.E.V.8
Ashley, S.E.9
Cairnduff, F.10
-
24
-
-
0031045148
-
Phase I trial and pharmacokinetics of the tubulin inhibitor 1069c85, a synthetic agent binding at the colchicine site designed to overcome multidrug resistance
-
Judson I, Briasoulis E, Raynaud F, Hanwell J, Berry C and Lacey H (1997) Phase I trial and pharmacokinetics of the tubulin inhibitor 1069C85, a synthetic agent binding at the colchicine site designed to overcome multidrug resistance. Br J Cancer 75: 608-613
-
(1997)
Br J Cancer
, vol.75
, pp. 608-613
-
-
Judson, I.1
Briasoulis, E.2
Raynaud, F.3
Hanwell, J.4
Berry, C.5
Lacey, H.6
-
25
-
-
0022529486
-
Phase I and pharmacokinetic study of LM975 (flavone acetic acid ester)
-
Kerr DJ, Kaye SB, Graham J, Cassidy J, Harding M, Setanoians A, McGrath JC, Vezin WR, Cunningham D, Forrest G and Soukop M (1986) Phase I and pharmacokinetic study of LM975 (flavone acetic acid ester). Cancer Res 46: 3142-3146
-
(1986)
Cancer Res
, vol.46
, pp. 3142-3146
-
-
Kerr, D.J.1
Kaye, S.B.2
Graham, J.3
Cassidy, J.4
Harding, M.5
Setanoians, A.6
McGrath, J.C.7
Vezin, W.R.8
Cunningham, D.9
Forrest, G.10
Soukop, M.11
-
26
-
-
0023608388
-
Phase I and pharmacokinetic study of flavone acetic acid
-
Kerr DJ, Kaye SB, Cassidy J, Bradley C, Rankin EM, Adams L, Setanotans A, Young T, Forrest G, Soukop M and Clavel M (1987) Phase I and pharmacokinetic study of flavone acetic acid. Cancer Res 47: 6776-6781
-
(1987)
Cancer Res
, vol.47
, pp. 6776-6781
-
-
Kerr, D.J.1
Kaye, S.B.2
Cassidy, J.3
Bradley, C.4
Rankin, E.M.5
Adams, L.6
Setanotans, A.7
Young, T.8
Forrest, G.9
Soukop, M.10
Clavel, M.11
-
27
-
-
0029089517
-
A phase I and pharmacology study of an oral platinum complex, JM216: Dose-dependent pharmacokinetics with single-dose administration
-
McKeage MJ, Mistry P, Ward J, Boxall FE, Loh S, O'Neill C, Ellis P, Kelland LR, Morgan SE, Murrer B, Santabarbara P, Harrap KR and Judson IR (1995) A Phase I and pharmacology study of an oral platinum complex, JM216: dose-dependent pharmacokinetics with single-dose administration. Cancer Chemother Pharmacol 36: 451-458
-
(1995)
Cancer Chemother Pharmacol
, vol.36
, pp. 451-458
-
-
McKeage, M.J.1
Mistry, P.2
Ward, J.3
Boxall, F.E.4
Loh, S.5
O'Neill, C.6
Ellis, P.7
Kelland, L.R.8
Morgan, S.E.9
Murrer, B.10
Santabarbara, P.11
Harrap, K.R.12
Judson, I.R.13
-
28
-
-
0030742993
-
Phase I and pharmacokinetic study of an oral platinum complex given daily for 5 days in patients with cancer
-
McKeage MJ, Raynaud F, Ward J, Berry C, O'Dell D, Kelland LR, Murrer B, Santabarbara P, Harrap KR and Judson IK (1997) Phase I and pharmacokinetic study of an oral platinum complex given daily for 5 days in patients with cancer. J Clin Oncol 15: 2691-2700
-
(1997)
J Clin Oncol
, vol.15
, pp. 2691-2700
-
-
McKeage, M.J.1
Raynaud, F.2
Ward, J.3
Berry, C.4
O'Dell, D.5
Kelland, L.R.6
Murrer, B.7
Santabarbara, P.8
Harrap, K.R.9
Judson, I.K.10
-
29
-
-
0027499297
-
Model-guided determination of maximum tolerated dose in phase I clinical trials: Evidence for increased precision
-
Mick R and Ratain MJ (1993) Model-guided determination of maximum tolerated dose in Phase I clinical trials: evidence for increased precision. J Natl Cancer Inst 85; 217-223
-
(1993)
J Natl Cancer Inst
, vol.85
, pp. 217-223
-
-
Mick, R.1
Ratain, M.J.2
-
30
-
-
0029564253
-
Phase I and pharmacokinetic study of the water-soluble etoposide prodrug, etoposide phosphate (BMY-40481)
-
Milliard MJ, Newell DR, Mummaneni V, Igwemezie LN, Balmanno K, Charlton CJ, Gumbrell L. Lind MJ, Chapman F, Proctor M, Simmonds D, Cantwell BMJ, Taylor GA, McDaniel C, Winograd B, Kaul S, Barbaiya RH and Calvert AH (1995) Phase I and pharmacokinetic study of the water-soluble etoposide prodrug, etoposide phosphate (BMY-40481). Eur J Cancer 31A: 2409-2411
-
(1995)
Eur J Cancer
, vol.31 A
, pp. 2409-2411
-
-
Milliard, M.J.1
Newell, D.R.2
Mummaneni, V.3
Igwemezie, L.N.4
Balmanno, K.5
Charlton, C.J.6
Gumbrell, L.7
Lind, M.J.8
Chapman, F.9
Proctor, M.10
Simmonds, D.11
Cantwell, B.M.J.12
Taylor, G.A.13
McDaniel, C.14
Winograd, B.15
Kaul, S.16
Barbaiya, R.H.17
Calvert, A.H.18
-
31
-
-
0021924337
-
Phase I clinical trial of mitozolomide
-
Newlands ES, Blackledge G, Slack JA, Goddard C, Brindley CJ, Holden L and Stevens MFG (1985) Phase I clinical trial of mitozolomide. Cancer Treat Rep 69: 801-805
-
(1985)
Cancer Treat Rep
, vol.69
, pp. 801-805
-
-
Newlands, E.S.1
Blackledge, G.2
Slack, J.A.3
Goddard, C.4
Brindley, C.J.5
Holden, L.6
Stevens, M.F.G.7
-
32
-
-
0026513077
-
Phase I trial of temozolomide (CCRG 81045; M&B 39831; NSC 362856)
-
Newlands ES, Blackledge GRP, Slack JA, Rustin GJS, Smith DB, Stuart NSA, Quarterman CP, Hoffman R, Stevens MFG, Brampton MH and Gibson AC (1992) Phase I trial of temozolomide (CCRG 81045; M&B 39831; NSC 362856). Br J Cancer 65: 287-291
-
(1992)
Br J Cancer
, vol.65
, pp. 287-291
-
-
Newlands, E.S.1
Blackledge, G.R.P.2
Slack, J.A.3
Rustin, G.J.S.4
Smith, D.B.5
Stuart, N.S.A.6
Quarterman, C.P.7
Hoffman, R.8
Stevens, M.F.G.9
Brampton, M.H.10
Gibson, A.C.11
-
34
-
-
0025986460
-
Methods for dose finding studies in cancer clinical trials: A review and results of a Monte Carlo study
-
O'Quigley J and Chevrel S (1991) Methods for dose finding studies in cancer clinical trials: a review and results of a Monte Carlo study. Stat Med 10: 1647-1664
-
(1991)
Stat Med
, vol.10
, pp. 1647-1664
-
-
O'Quigley, J.1
Chevrel, S.2
-
35
-
-
0018707237
-
Mouse and large animal toxicology studies of twelve antitumour agents: Relevance to starting dose for phase I clinical trials
-
Penta JS, Rozeneweig M, Guarino AM and Muggia FM (1979) Mouse and large animal toxicology studies of twelve antitumour agents: relevance to starting dose for Phase I clinical trials. Cancer Chemother Pharmacol 3: 97-101
-
(1979)
Cancer Chemother Pharmacol
, vol.3
, pp. 97-101
-
-
Penta, J.S.1
Rozeneweig, M.2
Guarino, A.M.3
Muggia, F.M.4
-
36
-
-
0026455160
-
Choice of starting dose and escalation for phase I studies of antitumour agents
-
Penta JS, Rosner GL and Trump DL (1992) Choice of starting dose and escalation for Phase I studies of antitumour agents. Cancer Chemother Pharmacol 31: 247-250
-
(1992)
Cancer Chemother Pharmacol
, vol.31
, pp. 247-250
-
-
Penta, J.S.1
Rosner, G.L.2
Trump, D.L.3
-
37
-
-
0027489606
-
Phase I study of bryostatin 1 : Assessment of interleukin 6 and tumour necrosis factor α induction in vivo
-
Phillip PA, Rea D, Thavasu P, Carmichael J, Stuart NSA, Rockett H, Talbot DC, Ganesan T, Pettit GR, Balkwill F and Harris AL (1993) Phase I study of bryostatin 1 : assessment of interleukin 6 and tumour necrosis factor α induction in vivo. J Natl Cancer Inst 85: 1812-1818
-
(1993)
J Natl Cancer Inst
, vol.85
, pp. 1812-1818
-
-
Phillip, P.A.1
Rea, D.2
Thavasu, P.3
Carmichael, J.4
Stuart, N.S.A.5
Rockett, H.6
Talbot, D.C.7
Ganesan, T.8
Pettit, G.R.9
Balkwill, F.10
Harris, A.L.11
-
38
-
-
0027326957
-
A phase I study of intravenous bryostatin 1 in patients with advanced cancer
-
Prendiville J, Crowther D, Thatcher N, Woll PJ, Fox BW, McGown A. Testa N, Stem P, McDermott R, Potter M and Pettit GR (1993) A Phase I study of intravenous bryostatin 1 in patients with advanced cancer. Br J Cancer 68: 418-424
-
(1993)
Br J Cancer
, vol.68
, pp. 418-424
-
-
Prendiville, J.1
Crowther, D.2
Thatcher, N.3
Woll, P.J.4
Fox, B.W.5
McGown, A.6
Testa, N.7
Stem, P.8
McDermott, R.9
Potter, M.10
Pettit, G.R.11
-
39
-
-
0028839152
-
Clinical pharmacokinetic and pharmacodynamic studies with the nonclassical antifolate thymidylate synthase inhibitor 3,4-dihydro-2-amino-6-methyl-4-oxo-5-(4 pyridylthio)-quinazoline dihydrochloride (AG337) given hy 24-hour intravenous infusion
-
Rafi I, Taylor GA, Calvete JA, Boddy AV, Batmanno K, Bailey N, Lind M, Calvert AH, Webber S, Jackson RJ, Johnston A, Clendeninn N and Newell DR (1995) Clinical pharmacokinetic and pharmacodynamic studies with the nonclassical antifolate thymidylate synthase inhibitor 3,4-dihydro-2-amino-6-methyl-4-oxo-5-(4 pyridylthio)-quinazoline dihydrochloride (AG337) given hy 24-hour intravenous infusion. Clin Cancer Res 1: 1275-1284
-
(1995)
Clin Cancer Res
, vol.1
, pp. 1275-1284
-
-
Rafi, I.1
Taylor, G.A.2
Calvete, J.A.3
Boddy, A.V.4
Batmanno, K.5
Bailey, N.6
Lind, M.7
Calvert, A.H.8
Webber, S.9
Jackson, R.J.10
Johnston, A.11
Clendeninn, N.12
Newell, D.R.13
-
40
-
-
0031934445
-
Preclinical and phase I clinical studies with the non-classical antifolate thymidylate synthase inhibitor nolatrexed dihydrochloride given by prolonged administration in patients with solid tumours
-
Rali I, Boddy AV, Calvete JA, Taylor GA, Newell DR, Bailey NP, Lind MJ, Green M, Hine J, Johnston A, Clendeninn N and Calvert A11 (1998) Preclinical and Phase I clinical studies with the non-classical antifolate thymidylate synthase inhibitor nolatrexed dihydrochloride given by prolonged administration in patients with solid tumours. J Clin Oncol 16: 1131-1141
-
(1998)
J Clin Oncol
, vol.16
, pp. 1131-1141
-
-
Rali, I.1
Boddy, A.V.2
Calvete, J.A.3
Taylor, G.A.4
Newell, D.R.5
Bailey, N.P.6
Lind, M.J.7
Green, M.8
Hine, J.9
Johnston, A.10
Clendeninn, N.11
Calvert, A.12
-
41
-
-
0027524863
-
Statistical and ethical issues in the design and conduct of phase I and phase II clinical trials of new anticancer agents
-
Ratain MJ, Mick R, Schilsky RL and Siegler M (1993) Statistical and ethical issues in the design and conduct of Phase I and Phase II clinical trials of new anticancer agents. J Natl Cancer Inst 85: 1637-1643
-
(1993)
J Natl Cancer Inst
, vol.85
, pp. 1637-1643
-
-
Ratain, M.J.1
Mick, R.2
Schilsky, R.L.3
Siegler, M.4
-
42
-
-
0019421081
-
Animal toxicology for early clinical trials with anticancer agents
-
Rozeneweig M, Von Hoff DD, Staquet MJ, Schein PS, Penta JS, Goldin A, Muggia FM, Freireich EJ and DeVite VT (1981) Animal toxicology for early clinical trials with anticancer agents. Cancer Clin Trials 4: 21-28
-
(1981)
Cancer Clin Trials
, vol.4
, pp. 21-28
-
-
Rozeneweig, M.1
Von Hoff, D.D.2
Staquet, M.J.3
Schein, P.S.4
Penta, J.S.5
Goldin, A.6
Muggia, F.M.7
Freireich, E.J.8
Devite, V.T.9
-
43
-
-
0030749549
-
Accelerated titration designs for phase I clinical trials in oncology
-
Simon R, Freidlin B, Rubinstein L, Arbuck S, Collins J and Christian MC (1997) Accelerated titration designs for Phase I clinical trials in oncology. J Natl Cancer Inst 89: 1138-1147
-
(1997)
J Natl Cancer Inst
, vol.89
, pp. 1138-1147
-
-
Simon, R.1
Freidlin, B.2
Rubinstein, L.3
Arbuck, S.4
Collins, J.5
Christian, M.C.6
-
44
-
-
0023261792
-
Phase I clinical trial of methylene dimethyl sulfonate
-
Smith DB, Fox BW, Thatcher N, Steward WP, Scarffe JH, Wagstaff J, Vezin R and Crowther D (1987) Phase I clinical trial of methylene dimethyl sulfonate. Cancer Treat Rep 71: 817-820
-
(1987)
Cancer Treat Rep
, vol.71
, pp. 817-820
-
-
Smith, D.B.1
Fox, B.W.2
Thatcher, N.3
Steward, W.P.4
Scarffe, J.H.5
Wagstaff, J.6
Vezin, R.7
Crowther, D.8
-
45
-
-
0023941535
-
A phase I trial and pharmacokinetic study of amphethinite
-
Smith DB, Ewen C, MacKintosh J, Fox BW, Thatcher N, Scarffe JH, Vezin R and Crowther D (1988) A Phase I trial and pharmacokinetic study of amphethinite. Br J Cancer 57: 023-627
-
(1988)
Br J Cancer
, vol.57
, pp. 23-627
-
-
Smith, D.B.1
Ewen, C.2
Mackintosh, J.3
Fox, B.W.4
Thatcher, N.5
Scarffe, J.H.6
Vezin, R.7
Crowther, D.8
-
46
-
-
0024536104
-
A phase I study of meta-azidopyrimethamine etanesulphonate (MZPES): A new dihydrofolate reductase inhibitor
-
Stuart NSA, Crawford SM, Blackledge GRP, Newlands ES, Slack J, Hoffman R and Stevens MFG (1989) A Phase I study of meta-azidopyrimethamine etanesulphonate (MZPES): a new dihydrofolate reductase inhibitor. Cancer Chemother Pharmacol 23: 308-310
-
(1989)
Cancer Chemother Pharmacol
, vol.23
, pp. 308-310
-
-
Stuart, N.S.A.1
Crawford, S.M.2
Blackledge, G.R.P.3
Newlands, E.S.4
Slack, J.5
Hoffman, R.6
Stevens, M.F.G.7
-
47
-
-
0032959549
-
-
Vasey PA, Kaye SB, Morrison R, Twelves C, Wilson P, Duncan R, Thomson AH, Murray LS, Hilditch TE, Murray T, Burtles S, Fraier D, Frigerio E and Cassidy J (1999) Clin Cancer Res 5: 83-94
-
(1999)
Clin Cancer Res
, vol.5
, pp. 83-94
-
-
Vasey, P.A.1
Kaye, S.B.2
Morrison, R.3
Twelves, C.4
Wilson, P.5
Duncan, R.6
Thomson, A.H.7
Murray, L.S.8
Hilditch, T.E.9
Murray, T.10
Burtles, S.11
Fraier, D.12
Frigerio, E.13
Cassidy, J.14
-
48
-
-
0023693722
-
A phase I and pharmacokinetic study of didox: A ribonucleotide reductase inhibitor
-
Veale D, Carmichael J, Cuntwell BMJ, Elford BL, Blackie R, Kerr DJ, Kaye SB and Harris AL (1988) A Phase I and pharmacokinetic study of didox: a ribonucleotide reductase inhibitor. Br J Cancer 58: 70-72
-
(1988)
Br J Cancer
, vol.58
, pp. 70-72
-
-
Veale, D.1
Carmichael, J.2
Cuntwell, B.M.J.3
Elford, B.L.4
Blackie, R.5
Kerr, D.J.6
Kaye, S.B.7
Harris, A.L.8
-
49
-
-
0009527432
-
Starting dose levels for phase I studies
-
Verweij J (1996) Starting dose levels for Phase I studies. Ann Oncol 7 (suppl. 1): 13
-
(1996)
Ann Oncol
, vol.7
, Issue.SUPPL. 1
, pp. 13
-
-
Verweij, J.1
|