- |||||||||| Stivarga (regorafenib) / Bayer
Biomarker, Trial completion, Trial primary completion date: RegoRec: Biomolecular Analysis for Predicting Response to Regorafenib (clinicaltrials.gov) - Mar 13, 2025 P=N/A, N=53, Completed, These results, alongside the published TRIDENT-1 clinical data, further support repotrectinib as a potential new standard of care for TKI-na Recruiting --> Completed | Trial primary completion date: Jun 2024 --> Sep 2024
- |||||||||| Ensacove (ensartinib) / Betta Pharma
Journal, PD(L)-1 Biomarker, IO biomarker: Ensartinib as a neoadjuvant therapy for stage IIIA non-small cell lung cancer patients with EML4-ALK fusion: a case report and literature review. (Pubmed Central) - Mar 12, 2025 Nevertheless, clinical trials can be conducted in the future to validate our results. Moreover, we performed multiple immunofluorescence staining analyses on samples before and after neoadjuvant therapy, observed and compared the changes in the expression of relevant immune cells (CD8+ T cells, macrophages, PD-1, and PD-L1), and performed a simple analysis.
- |||||||||| Augtyro (repotrectinib) / BMS
Trial completion date, Trial primary completion date: CA127-1072: A Study to Assess the Effect of Voriconazole and Quinidine on the Pharmacokinetics of a Single Dose of Repotrectinib in Healthy Participants (clinicaltrials.gov) - Mar 12, 2025 P1, N=32, Recruiting, Moreover, we performed multiple immunofluorescence staining analyses on samples before and after neoadjuvant therapy, observed and compared the changes in the expression of relevant immune cells (CD8+ T cells, macrophages, PD-1, and PD-L1), and performed a simple analysis. Trial primary completion date: Dec 2024 --> Jul 2025 | Trial completion date: Dec 2024 --> Jul 2025
- |||||||||| Vitrakvi (larotrectinib) / Bayer
Journal, MSi-H Biomarker: Efficacy and safety of larotrectinib in patients with TRK fusion gastrointestinal cancer. (Pubmed Central) - Mar 12, 2025 P2 Larotrectinib demonstrated long durability, extended survival and manageable safety in patients with TRK fusion GI cancer, including those with MSI-H CRC. This supports the wider adoption of next-generation sequencing testing for NTRK gene fusions in patients with GI cancer.
- |||||||||| Mekinist (trametinib) / Novartis, BeiGene, Gavreto (pralsetinib) / Rigel, Tafinlar (dabrafenib) / Novartis
FDA event, Journal, Monotherapy: Monotherapy vs combination therapy evaluation of FDA-approved TKIs targeting PDGFR for the treatment of thyroid cancer. (Pubmed Central) - Mar 10, 2025 On 4th May, 2018, a combination of Dabrafenib and Trametinib/Dab-Tra has been approved by US FDA for the treatment of anaplastic thyroid cancer (ATC) that highlights the importance of combination therapy in its treatment...We found that the best combination amongst all is of Pralsetinib and Trametinib/Pra-Tra with a docking score of -14.47?kcal/mol...We also found that a combinatorial approach with TKIs could prove to be better than monotherapy. Further in-vitro and in-vivo studies are required to strengthen the results obtained through in-silico experiment.
- |||||||||| Biomarker, Review, Journal, Tumor mutational burden, PD(L)-1 Biomarker, Pan tumor: Pan-Cancer Molecular Biomarkers: Practical Considerations for the Surgical Pathologist. (Pubmed Central) - Mar 10, 2025
Several other biomarkers are currently under investigation including FGFR, RET, and ROS1 fusions; ERBB2 amplification; and mutations in the AKT1/2/3, NF1, RAS pathway, and MAPK pathway. As molecular assays are increasingly incorporated into routine tumor workup, the emergence of additional pan-cancer biomarkers is likely to be a matter more of "when" than "if." In this review, we first explore some of the conceptual and technical considerations at the intersection of surgical and molecular pathology, followed by a brief overview of both established and emerging molecular pan-cancer biomarkers and their diagnostic and clinical applications.
- |||||||||| Stivarga (regorafenib) / Bayer
Preclinical, Journal: Regorafenib as a potential drug for severe COVID-19: inhibition of inflammasome activation in mice. (Pubmed Central) - Mar 10, 2025 Notably, regorafenib inhibited NLR family pyrin domain containing 3 (NLRP3) inflammasome activation, a key driver of the cytokine storm associated with severe COVID-19. Our findings elucidate the molecular mechanisms underlying therapeutic effects of regorafenib and suggest its potential use as a promising treatment option for severe COVID-19.
- |||||||||| Rozlytrek (entrectinib) / Roche, Alecensa (alectinib) / Roche
HORIZON-01: a phase I (0) - Mar 7, 2025 - Abstract #BTOG2025BTOG_408; P2, P3 Eligible patients are randomised 1: 1 to receive durvalumab (one year) or targeted therapy (three years) including alectinib (ALK+) or entrectinib (ROS1+), until disease progression, maximum treatment duration, unacceptable toxicity, consent withdrawal, or death. N/A.
- |||||||||| Enrollment closed, Trial primary completion date: Cabozantinib in Combo with NIVO + IPI in Advanced NCCRCC (clinicaltrials.gov) - Mar 3, 2025
P2, N=60, Active, not recruiting, No abstract available Recruiting --> Active, not recruiting | Trial primary completion date: Dec 2024 --> Jun 2025
- |||||||||| Clinical protocol, P2 data, Journal: Raltitrexed, S-1 and fruquintinib (RSF) in the treatment of refractory metastatic colorectal cancer: study protocol for a multicenter, prospective, single-arm, phase II trial. (Pubmed Central) - Mar 1, 2025
P2 By leveraging complementary mechanisms of action, this study aims to optimize therapeutic outcomes in heavily pretreated patients. Further clinical research is essential to validate efficacy, safety, and potential biomarkers for patient selection.
- |||||||||| Journal, Adverse events: HOPIPRAC: Pharmacovigilance interface for detecting cases of adverse events in a hospital data warehouse (Pubmed Central) - Feb 27, 2025
The HOPIPRAC interface gives pharmacovigilants autonomy in monitoring drug risk in healthcare institutions, in addition to spontaneous notification. Querying a more advanced warehouse that collects multimodal data, and deploying it on a wider regional or even national scale, will help to overcome some of the limitations of the current warehouse.
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