^
2ms
A Study to Learn About the Study Medicine Called PF-07799933 in People With Advanced Solid Tumors With BRAF Alterations. (clinicaltrials.gov)
P1, N=174, Recruiting, Pfizer | Trial completion date: May 2027 --> Dec 2028 | Trial primary completion date: Nov 2025 --> Jun 2027
Trial completion date • Trial primary completion date • Combination therapy • Metastases
|
BRAF (B-raf proto-oncogene)
|
Erbitux (cetuximab) • Mektovi (binimetinib) • PF-07799933
3ms
Trial completion date • Combination therapy • Metastases
|
BRAF (B-raf proto-oncogene)
|
Erbitux (cetuximab) • Mektovi (binimetinib) • PF-07799933
6ms
Trial completion date • Combination therapy • Metastases
|
BRAF (B-raf proto-oncogene) • CYP3A4 (Cytochrome P450, family 3, subfamily A, polypeptide 4)
|
Erbitux (cetuximab) • Mektovi (binimetinib) • PF-07799933
7ms
A Study to Learn About the Study Medicine Called PF-07799933 in People With Advanced Solid Tumors. (clinicaltrials.gov)
P1, N=174, Recruiting, Pfizer | Trial completion date: Jan 2028 --> Apr 2027 | Trial primary completion date: Jul 2026 --> Oct 2025
Trial completion date • Trial primary completion date • Combination therapy • Metastases
|
BRAF (B-raf proto-oncogene) • CYP3A4 (Cytochrome P450, family 3, subfamily A, polypeptide 4)
|
Erbitux (cetuximab) • Mektovi (binimetinib) • PF-07799933
1year
A phase 1, open-label, dose escalation and dose expansion study to evaluate the safety, tolerability, pharmacokinetics, and antitumor activity of PF-07799933 (ARRY-440) as a single agent and in combination therapy in participants 16 years and older with advanced solid tumors with BRAF alterations. (ASCO 2023)
We describe here the Phase 1 study of PF-07799933 as monotherapy or in combination with binimetinib or cetuximab in participants with BRAF-altered advanced solid tumors. The primary objective of Part 3 is efficacy in defined cohorts (total ~120 participants): Cohort 1-2: BRAF V600 mutant melanoma; Cohort 3: BRAF Class II altered melanoma; Cohorts 4-5: BRAF V600 and Class II altered CRC; Cohort 6: other BRAF V600, Class II/III altered solid tumor not qualifying for Cohorts 1-5. Clinical trial information: NCT05355701.
Clinical • P1 data • PK/PD data • Combination therapy • Metastases
|
BRAF (B-raf proto-oncogene)
|
BRAF mutation • BRAF amplification
|
Erbitux (cetuximab) • Mektovi (binimetinib) • PF-07799933
1year
A Study to Learn About the Study Medicine Called PF-07799544 in People With Advanced Solid Tumors (clinicaltrials.gov)
P1, N=124, Recruiting, Pfizer | Trial completion date: Dec 2027 --> Jun 2027 | Trial primary completion date: Sep 2026 --> Jan 2026
Trial completion date • Trial primary completion date • Combination therapy • Metastases
|
BRAF (B-raf proto-oncogene)
|
BRAF mutation • BRAF V600
|
Braftovi (encorafenib) • tinlorafenib (PF-07284890) • PF-07799544 • PF-07799933
over1year
Enrollment open • Combination therapy • Metastases
|
BRAF (B-raf proto-oncogene)
|
BRAF mutation • BRAF V600
|
Braftovi (encorafenib) • tinlorafenib (PF-07284890) • PF-07799544 • PF-07799933
over1year
A Study to Learn About the Study Medicine Called PF-07799544 in People With Advanced Solid Tumors (clinicaltrials.gov)
P1, N=124, Not yet recruiting, Pfizer | Trial primary completion date: May 2026 --> Aug 2026
Trial primary completion date • Combination therapy • Metastases
|
BRAF (B-raf proto-oncogene)
|
BRAF mutation • BRAF V600
|
Braftovi (encorafenib) • tinlorafenib (PF-07284890) • PF-07799544 • PF-07799933
over1year
New P1 trial • Combination therapy
|
BRAF (B-raf proto-oncogene)
|
BRAF mutation • BRAF V600
|
Braftovi (encorafenib) • tinlorafenib (PF-07284890) • PF-07799544 • PF-07799933
over1year
Enrollment open • Combination therapy
|
BRAF (B-raf proto-oncogene) • CYP3A4 (Cytochrome P450, family 3, subfamily A, polypeptide 4)
|
Erbitux (cetuximab) • Mektovi (binimetinib) • PF-07799933
2years
New P1 trial • Combination therapy
|
BRAF (B-raf proto-oncogene) • CYP3A4 (Cytochrome P450, family 3, subfamily A, polypeptide 4)
|
Erbitux (cetuximab) • Mektovi (binimetinib) • PF-07799933