Adam W. Cook
Research Subjects
Adam W. Cook has a total of 24 co-authors. Here are the top co-authors by number of shared publications:
- Alexander Drilon
Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, USA
86 shared publications - Allison S. Harney
Albert Einstein College of Medicine, Bronx, NY
86 shared publications - Anurag Singh
Pfizer Boulder Research and Development, Boulder, Colorado. 11
86 shared publications - Christina E. Wong
Pfizer Boulder Research Unit, Boulder, Colorado
86 shared publications - Dale Nepert
Pfizer Boulder Research Unit, Boulder, Colorado
86 shared publications - Dylan P. Hartley
Pfizer Boulder Research and Development, Boulder, Colorado. 11
86 shared publications
Latest Publications
- Open Access
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Table S8 from SHP2 Inhibition Sensitizes Diverse Oncogene-Addicted Solid Tumors to Re-treatment with Targeted Therapy
Supplementary Table 8: Comparison of clinical safety data for SHP2 inhibitors
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Open AccessTable S8 from SHP2 Inhibition Sensitizes Diverse Oncogene-Addicted Solid Tumors to Re-treatment with Targeted Therapy
Supplementary Table 8: Comparison of clinical safety data for SHP2 inhibitors
- Open Access
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Table S2 from SHP2 Inhibition Sensitizes Diverse Oncogene-Addicted Solid Tumors to Re-treatment with Targeted Therapy
Supplementary Table 2: Phosphatase Profiling of PF-07284892
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Open AccessTable S2 from SHP2 Inhibition Sensitizes Diverse Oncogene-Addicted Solid Tumors to Re-treatment with Targeted Therapy
Supplementary Table 2: Phosphatase Profiling of PF-07284892
- Open Access
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Figure S3 from SHP2 Inhibition Sensitizes Diverse Oncogene-Addicted Solid Tumors to Re-treatment with Targeted Therapy
Supplementary Figure 3: Preclinical development of PF-07284892
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Open AccessFigure S3 from SHP2 Inhibition Sensitizes Diverse Oncogene-Addicted Solid Tumors to Re-treatment with Targeted Therapy
Supplementary Figure 3: Preclinical development of PF-07284892
- Open Access
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Figure S6 from SHP2 Inhibition Sensitizes Diverse Oncogene-Addicted Solid Tumors to Re-treatment with Targeted Therapy
Supplementary Figure 6: PK profiles for patients
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Open AccessFigure S6 from SHP2 Inhibition Sensitizes Diverse Oncogene-Addicted Solid Tumors to Re-treatment with Targeted Therapy
Supplementary Figure 6: PK profiles for patients
- Open Access
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Table S3 from SHP2 Inhibition Sensitizes Diverse Oncogene-Addicted Solid Tumors to Re-treatment with Targeted Therapy
Supplementary Table 3: IC50 values for PF-07284892 in cell-based assays
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Open AccessTable S3 from SHP2 Inhibition Sensitizes Diverse Oncogene-Addicted Solid Tumors to Re-treatment with Targeted Therapy
Supplementary Table 3: IC50 values for PF-07284892 in cell-based assays
- Open Access
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Figure S5 from SHP2 Inhibition Sensitizes Diverse Oncogene-Addicted Solid Tumors to Re-treatment with Targeted Therapy
Supplementary Figure 5: Study schema
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Open AccessFigure S5 from SHP2 Inhibition Sensitizes Diverse Oncogene-Addicted Solid Tumors to Re-treatment with Targeted Therapy
Supplementary Figure 5: Study schema
- Open Access
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Table S6 from SHP2 Inhibition Sensitizes Diverse Oncogene-Addicted Solid Tumors to Re-treatment with Targeted Therapy
Supplementary Table 6: Disposition of all patients enrolled to Dose Level 1
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Open AccessTable S6 from SHP2 Inhibition Sensitizes Diverse Oncogene-Addicted Solid Tumors to Re-treatment with Targeted Therapy
Supplementary Table 6: Disposition of all patients enrolled to Dose Level 1
- Open Access
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Table S7 from SHP2 Inhibition Sensitizes Diverse Oncogene-Addicted Solid Tumors to Re-treatment with Targeted Therapy
Supplementary Table 7: Adverse events for Dose Level 1 patients
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Open AccessTable S7 from SHP2 Inhibition Sensitizes Diverse Oncogene-Addicted Solid Tumors to Re-treatment with Targeted Therapy
Supplementary Table 7: Adverse events for Dose Level 1 patients
- Open Access
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Figure S1 from SHP2 Inhibition Sensitizes Diverse Oncogene-Addicted Solid Tumors to Re-treatment with Targeted Therapy
Supplementary Figure 1: Comparison of the structures of PF-07284892, RMC445507, TNO155 bound to SHP2
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Open AccessFigure S1 from SHP2 Inhibition Sensitizes Diverse Oncogene-Addicted Solid Tumors to Re-treatment with Targeted Therapy
Supplementary Figure 1: Comparison of the structures of PF-07284892, RMC445507, TNO155 bound to SHP2
- Open Access
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Figure S2 from SHP2 Inhibition Sensitizes Diverse Oncogene-Addicted Solid Tumors to Re-treatment with Targeted Therapy
Supplementary Figure 2: Intermittent dosing of PF-07284892 preserves efficacy and improves tolerability preclinically
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Open AccessFigure S2 from SHP2 Inhibition Sensitizes Diverse Oncogene-Addicted Solid Tumors to Re-treatment with Targeted Therapy
Supplementary Figure 2: Intermittent dosing of PF-07284892 preserves efficacy and improves tolerability preclinically