- |||||||||| AiTan (rivoceranib) / HLB Bio Group, Avastin (bevacizumab) / Roche
Journal: JAK3/STAT5A-dependent IL-8 regulation drives ESCC angiogenesis and is suppressed by dihydroartemisinin. (Pubmed Central) - Jul 16, 2025 Besides, DHA inhibited ESCC angiogenesis through JAK3/STAT5A/IL-8 signaling in vivo and in vitro, and JAK3 blockade alleviated its effect. In conclusion, these findings demonstrate a critical role of the JAK3/STAT5A/IL-8 pathway in regulating ESCC angiogenesis, and DHA is an effective drug for targeting JAK3 against ESCC angiogenesis, providing a research basis and a new strategy for anti-ESCC angiogenesis therapy.
- |||||||||| Jardiance (empagliflozin) / Eli Lilly, Boehringer Ingelheim, Ruiqin (henagliflozin) / Jiangsu Hengrui Pharma, sorafenib / Generic mfg.
PK/PD data, Preclinical, Journal: In vivo assessment of pharmacokinetic interactions of empagliflozin and henagliflozin with sorafenib: an animal-based study. (Pubmed Central) - Jul 14, 2025 Empagliflozin and henagliflozin inhibited Oatp1b2 expression in the liver and P-gp expression in the liver and intestines. These pharmacokinetic interactions provide valuable insights for future studies on optimizing the dosing regimens of sorafenib in combination with empagliflozin or henagliflozin, potentially reducing toxicity risks and improving the safety of coadministration in clinical settings.
- |||||||||| oxaliplatin / Generic mfg., Teysuno (gimeracil/oteracil/tegafur) / Nordic Group, Otsuka, AiRuiKa (camrelizumab) / HLB Bio Group
P2 data, Journal: Camrelizumab plus SOX chemotherapy as adjuvant therapy for pathological stage III gastric or gastroesophageal junction adenocarcinoma: a prospective, multicenter, single-arm, phase II trial. (Pubmed Central) - Jul 14, 2025 P2 However, careful patient selection is necessary to identify patients most likely to benefit from combination therapy. ClinicalTrials.gov registry: NCT04515615; Date of registration: August 14, 2020; Weblink: https://clinicaltrials.gov/study/NCT04515615.
- |||||||||| Tevimbra (tislelizumab-jsgr) / BeOne Medicines, AiRuiKa (camrelizumab) / HLB Bio Group
Trial completion date, Trial primary completion date, Checkpoint inhibition: Efficacy and Safety of Super-hyperfractionation Pulse Radiotherapy Combined With ICIs for Advanced NSCLC (clinicaltrials.gov) - Jul 14, 2025 P=N/A, N=40, Recruiting, ClinicalTrials.gov registry: NCT04515615; Date of registration: August 14, 2020; Weblink: https://clinicaltrials.gov/study/NCT04515615. Trial completion date: Mar 2025 --> Mar 2026 | Trial primary completion date: Mar 2025 --> Mar 2026
- |||||||||| Teysuno (gimeracil/oteracil/tegafur) / Nordic Group, Otsuka
Journal, Adverse events, Tumor mutational burden, PARP Biomarker, PD(L)-1 Biomarker, IO biomarker: Prolonged Progression-Free Survival in a Patient with Highly Pretreated Recurrent Ovarian Cancer after Developing Multisystem Immune-Related Adverse Events: A Case Report and Literature Review. (Pubmed Central) - Jul 11, 2025 From May 2022, the patient was switched to maintenance therapy with tislelizumab plus olaparib...We report a case involving a patient with highly pretreated recurrent ovarian cancer who exhibited prolonged PFS after developing three irAEs. The distinctly prolonged PFS observed, along with the reviewed literature, suggests that irAEs may be correlated with improved survival in ovarian cancer.
- |||||||||| AnDaJing (vunakizumab) / Jiangsu Hengrui Pharma
Enrollment open, Trial completion date, Trial primary completion date: Vunakizumab for the Treatment of Mild to Moderate Systemic Lupus Erythematosus (clinicaltrials.gov) - Jul 10, 2025 P1, N=20, Recruiting, Recruiting --> Active, not recruiting | Trial completion date: Dec 2024 --> Dec 2025 | Trial primary completion date: Dec 2023 --> Dec 2025 Not yet recruiting --> Recruiting | Trial completion date: Apr 2027 --> Dec 2027 | Trial primary completion date: Oct 2025 --> Nov 2026
- |||||||||| Review, Journal: A momentous progress update: epidermal growth factor receptor inhibitors as viable agents for combating cancer. (Pubmed Central) - Jul 9, 2025
Preclinical, clinical, structure-activity relationships (SAR) with mechanism-based and in silico research, and other relevant data are compiled to offer directions for the scientific discovery of novel EGFR inhibitors with conceivable uses in therapy. The research trajectory of this entire field will provide incessant opportunities for the discovery of novel drug molecules with improved efficacy and selectivity.
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