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A phase 1, multicenter, dose-escalation study of PRN1371, an irreversible covalent FGFR1-4 kinase inhibitor, in patients with advanced solid tumors including metastatic urothelial carcinoma (mUC).

Conferences
Piha-Paul, SA; Hierro, C; Matos, I; Boni, V; Hahn, N; Bitting, R; Bauer, T; Rahul, A; Meric-Bernstam, F; Gourlay, S; Owens, TD; Brameld, K ...
Published in: CLINICAL CANCER RESEARCH
August 2020

Duke Scholars

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Published In

CLINICAL CANCER RESEARCH

EISSN

1557-3265

ISSN

1078-0432

Publication Date

August 2020

Volume

26

Issue

15

Start / End Page

40 / 41

Related Subject Headings

  • Oncology & Carcinogenesis
  • 3211 Oncology and carcinogenesis
  • 3202 Clinical sciences
 

Citation

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Piha-Paul, S. A., Hierro, C., Matos, I., Boni, V., Hahn, N., Bitting, R., … Tabernero, J. (2020). A phase 1, multicenter, dose-escalation study of PRN1371, an irreversible covalent FGFR1-4 kinase inhibitor, in patients with advanced solid tumors including metastatic urothelial carcinoma (mUC). In CLINICAL CANCER RESEARCH (Vol. 26, pp. 40–41).
Piha-Paul, Sarina A., Cinta Hierro, Ignacio Matos, Valentina Boni, Noah Hahn, Rhonda Bitting, Todd Bauer, et al. “A phase 1, multicenter, dose-escalation study of PRN1371, an irreversible covalent FGFR1-4 kinase inhibitor, in patients with advanced solid tumors including metastatic urothelial carcinoma (mUC).” In CLINICAL CANCER RESEARCH, 26:40–41, 2020.
Piha-Paul SA, Hierro C, Matos I, Boni V, Hahn N, Bitting R, Bauer T, Rahul A, Meric-Bernstam F, Gourlay S, Owens TD, Brameld K, Neale A, Schwartz R, Murray S, Ucpinar S, Foote P, Venetsanakos E, Tabernero J. A phase 1, multicenter, dose-escalation study of PRN1371, an irreversible covalent FGFR1-4 kinase inhibitor, in patients with advanced solid tumors including metastatic urothelial carcinoma (mUC). CLINICAL CANCER RESEARCH. 2020. p. 40–41.

Published In

CLINICAL CANCER RESEARCH

EISSN

1557-3265

ISSN

1078-0432

Publication Date

August 2020

Volume

26

Issue

15

Start / End Page

40 / 41

Related Subject Headings

  • Oncology & Carcinogenesis
  • 3211 Oncology and carcinogenesis
  • 3202 Clinical sciences