^
6ms
Safety, Efficacy, and Tolerability of BOS172738 in Patients With Advanced Rearranged During Transfection (RET) Gene-Altered Tumors (clinicaltrials.gov)
P1, N=117, Completed, Boston Pharmaceuticals | Active, not recruiting --> Completed | Trial completion date: Aug 2024 --> Sep 2023 | Trial primary completion date: Mar 2024 --> Sep 2023
Trial completion • Trial completion date • Trial primary completion date • Metastases
|
RET (Ret Proto-Oncogene)
|
RET fusion • RET mutation
|
zeteletinib (BOS-172738)
1year
Safety, Efficacy, and Tolerability of BOS172738 in Patients With Advanced Rearranged During Transfection (RET) Gene-Altered Tumors (clinicaltrials.gov)
P1, N=117, Active, not recruiting, Boston Pharmaceuticals | Trial completion date: Apr 2023 --> Aug 2024 | Trial primary completion date: Apr 2023 --> Mar 2024
Trial completion date • Trial primary completion date
|
RET (Ret Proto-Oncogene)
|
RET fusion • RET mutation
|
zeteletinib (BOS-172738)
over1year
Safety, Efficacy, and Tolerability of BOS172738 in Patients With Advanced Rearranged During Transfection (RET) Gene-Altered Tumors (clinicaltrials.gov)
P1, N=117, Active, not recruiting, Boston Pharmaceuticals | Trial completion date: Dec 2022 --> Apr 2023 | Trial primary completion date: Dec 2022 --> Apr 2023
Trial completion date • Trial primary completion date • Metastases
|
RET (Ret Proto-Oncogene)
|
RET fusion • RET mutation
|
zeteletinib (BOS-172738)
2years
Safety, Efficacy, and Tolerability of BOS172738 in Patients With Advanced Rearranged During Transfection (RET) Gene-Altered Tumors (clinicaltrials.gov)
P1, N=117, Active, not recruiting, Boston Pharmaceuticals | Trial completion date: Jun 2022 --> Dec 2022 | Trial primary completion date: Jun 2022 --> Dec 2022
Trial completion date • Trial primary completion date
|
RET (Ret Proto-Oncogene)
|
RET fusion • RET mutation
|
zeteletinib (BOS-172738)
over2years
Safety, Efficacy, and Tolerability of BOS172738 in Patients With Advanced Rearranged During Transfection (RET) Gene-Altered Tumors (clinicaltrials.gov)
P1, N=117, Active, not recruiting, Boston Pharmaceuticals | Trial primary completion date: Dec 2021 --> Jun 2022
Clinical • Trial primary completion date
|
RET (Ret Proto-Oncogene)
|
RET fusion • RET mutation
|
zeteletinib (BOS-172738)
over2years
Safety, Efficacy, and Tolerability of BOS172738 in Patients With Advanced Rearranged During Transfection (RET) Gene-Altered Tumors (clinicaltrials.gov)
P1, N=117, Active, not recruiting, Boston Pharmaceuticals | Recruiting --> Active, not recruiting | Trial completion date: Dec 2021 --> Jun 2022
Clinical • Enrollment closed • Trial completion date
|
RET (Ret Proto-Oncogene)
|
RET fusion • RET mutation
|
zeteletinib (BOS-172738)
3years
[VIRTUAL] BOS172738, a highly potent and selective RET inhibitor, for the treatment of RET-altered tumors including RET-fusion+ NSCLC and RET-mutant MTC: Phase 1 study results. (ASCO 2021)
BOS172738 is a highly potent and selective RET inhibitor with a differentiated safety profile and clinical activity against RET-altered tumors, including patients with brain metastases . BOS172738 continues to be evaluated in patients with NSCLC, MTC, and in patients previously treated with other selective RET inhibitors.
P1 data
|
RET (Ret Proto-Oncogene) • KDR (Kinase insert domain receptor)
|
RET fusion • RET mutation
|
zeteletinib (BOS-172738)
over3years
Safety, Efficacy, and Tolerability of BOS172738 in Patients With Advanced Rearranged During Transfection (RET) Gene-Altered Tumors (clinicaltrials.gov)
P1, N=114, Recruiting, Boston Pharmaceuticals | Trial completion date: Jun 2021 --> Nov 2021 | Trial primary completion date: Dec 2020 --> Nov 2021
Clinical • Trial completion date • Trial primary completion date
|
RET (Ret Proto-Oncogene)
|
RET fusion • RET mutation
|
zeteletinib (BOS-172738)