- |||||||||| Keytruda (pembrolizumab) / Merck (MSD), Lenvima (lenvatinib) / Eisai, Merck (MSD)
Trial suspension: Lenvatinib, Pembrolizumab, and Paclitaxel for Treatment of Recurrent Endometrial, Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Cancer (clinicaltrials.gov) - Sep 21, 2022 P2, N=38, Suspended, BEX4 can be targeted to improve the efficacy of lenvatinib plus immune checkpoint inhibitors. Recruiting --> Suspended
- |||||||||| Tuoyi (toripalimab) / Shanghai Junshi Biosci, Coherus Biosci, Lenvima (lenvatinib) / Eisai, Merck (MSD)
P2 data, Retrospective data, Clinical Trial,Phase II, Journal: Lenvatinib, toripalimab plus hepatic arterial infusion chemotherapy in patients with high-risk advanced hepatocellular carcinoma: A biomolecular exploratory, phase II trial. (Pubmed Central) - Sep 21, 2022 Lenvatinib, toripalimab and FOLFOX-HAIC showed safe and encouraging antitumour activity for advanced HCC with high-risk features. The levels of CCL28 and BTC might be the predictive biomarkers for the triple combination therapy.
- |||||||||| Welireg (belzutifan) / Merck (MSD), Lenvima (lenvatinib) / Eisai, Merck (MSD), Cabometyx (cabozantinib tablet) / Takeda, Exelixis, Ipsen
LITESPARK-011: a randomized, phase 3 study of belzutifan plus lenvatinib versus cabozantinib after anti–PD-1/PD-L1 therapy in patients with advanced renal cell carcinoma (Poster Hall, Board F4) - Sep 21, 2022 - Abstract #IKCS2022IKCS_140; P3 Primary end points are PFS per RECIST v1.1 by blinded independent central review (BICR) and OS; secondary end points include ORR and DOR per RECIST v1.1 by BICR and safety and tolerability. LITESPARK-011 is recruiting patients in Asia, Australia, Europe, North America, and South America.
- |||||||||| Lenvima (lenvatinib) / Eisai, Merck (MSD)
Journal: Lenvatinib-induced hypocalcaemia due to transient primary hypoparathyroidism. (Pubmed Central) - Sep 20, 2022 Though hypocalcaemia has been described as potential side effect of MKI treatment, this is the first report of a lenvatinib-induced primary hypoparathyroidism, in a patient with a documented normal parathyroid function after surgery. The periodical assessment of calcium-phosphorus metabolism is thus warranted to prevent this potentially lethal side effect, in both post-surgical hypoparathyroid and euparathyroid patients.
- |||||||||| Enrollment change, Trial completion date, Trial primary completion date: The Drug Rediscovery Protocol (DRUP Trial) (clinicaltrials.gov) - Sep 19, 2022
P2, N=1550, Recruiting, The shrinkage of tumor blood vessels in imaging analysis may be associated with improved prognosis; however, additional studies are still required. N=950 --> 1550 | Trial completion date: Dec 2022 --> Dec 2027 | Trial primary completion date: Aug 2022 --> Sep 2027
- |||||||||| Invokana (canagliflozin) / J&J, Daiichi Sankyo, Mitsubishi Tanabe
PK/PD data, Preclinical, Journal: Pharmacokinetic Interactions between Canagliflozin and Sorafenib or Lenvatinib in Rats. (Pubmed Central) - Sep 18, 2022 Canagliflozin caused a significant increase in AUC and C of lenvatinib by 28.9% and 36.2%, respectively, and a significant decrease in V and CL of lenvatinib by 52.9% and 22.7%, respectively. In conclusion, drug interactions exist between canagliflozin and sorafenib or lenvatinib, and these findings provide a reference for the use of these drugs in patients with HCC and T2DM.
- |||||||||| Retrospective data, Review: Efficacy and safety of targeted therapeutics for patients with radioiodine-refractory differentiated thyroid cancer: Systematic review and network meta-analysis. (Pubmed Central) - Sep 14, 2022
A total of 12 eligible RCTs involved 1,959 patients and 13 treatments: apatinib, cabozantinib, anlotinib, nintedanib, lenvatinib, lenvatinib with low dose (LD), sorafenib, sorafenib plus everolimus, donafenib (200 mg), donafenib (300 mg), pazopanib (continuous), pazopanib (intermittent), and vandetanib...Patients who received lenvatinib or apatinib also had more grade 3 or higher adverse events. Systematic Review Registration: [https://www.crd.york.ac.uk/PROSPERO/display_record.php?RecordID=302249], identifier [CRD42022302249].
|