- |||||||||| Neulasta (pegfilgrastim) / Amgen, Kyowa Hakko Kirin, Roche, Lonquex (lipegfilgrastim biosimilar) / Teva
Retrospective data, Review, Journal: Efficacy and tolerability of granulocyte colony-stimulating factors in cancer patients after chemotherapy: A systematic review and Bayesian network meta-analysis. (Pubmed Central) - Nov 2, 2020 Mecapegfilgrastim, balugrastim, lipegfilgrastim and L-G-CSF biosimilar were best G-CSF drugs in reducing BP (cumulative probabilities: 20%, 14%, 8%, 8%, respectively). Mecapegfilgrastim, lipegfilgrastim and balugrastim might be the most appreciate G-CSF drugs with both good efficacy and tolerability when treating cancer patients after cytotoxic chemotherapy.
- |||||||||| AiRuiKa (camrelizumab) / HLB Bio Group
Enrollment open, Trial completion date, Trial primary completion date: Microwave Ablation in Combination With Camrelizumab Versus Camrelizumab in Metastatic Non-small-cell Lung Cancer (clinicaltrials.gov) - Nov 1, 2020 P2, N=200, Recruiting, Mecapegfilgrastim, lipegfilgrastim and balugrastim might be the most appreciate G-CSF drugs with both good efficacy and tolerability when treating cancer patients after cytotoxic chemotherapy. Not yet recruiting --> Recruiting | Trial completion date: Feb 2021 --> Feb 2022 | Trial primary completion date: Oct 2020 --> Oct 2021
- |||||||||| Zaltrap (ziv-aflibercept IV) / Sanofi, Regeneron
Journal: VEGF Trap Suspended in the Semifluorinated Alkane F6H8 Inhibits Inflammatory Corneal Hem- and Lymphangiogenesis. (Pubmed Central) - Nov 1, 2020 The purpose of this study was to test the effect of vascular endothelial growth factor (VEGF) Trap suspended in the SFA perfluorohexyloctane (Trap/F6H8) on corneal neovascularization...Our findings might open new treatment avenues for local anti-angiogenic therapy at the cornea, as F6H8 is already approved for the usage at the ocular surface. With this study we show for the first time that SFAs can serve as carriers for anti-angiogenic drugs at the ocular surface.
- |||||||||| AiSuDa (ivarmacitinib) / Jiangsu Hengrui Pharma, Arcutis
Trial completion, Trial completion date, Trial primary completion date: A Phase II Study in Adult Patients With Moderate to Severe Atopic Dermatitis (clinicaltrials.gov) - Oct 29, 2020 P2, N=105, Completed, The combination of warfarin and imrecoxib did not impact the pharmacodynamics and pharmacokinetics of single-dose warfarin; therefore, when treating a patient with imrecoxib and warfarin, it is not required to adjust the dosage of warfarin. Recruiting --> Completed | Trial completion date: Dec 2020 --> Aug 2020 | Trial primary completion date: Dec 2020 --> Aug 2020
- |||||||||| AiSuDa (ivarmacitinib) / Jiangsu Hengrui Pharma, Arcutis
Enrollment open, Trial completion date, Trial primary completion date: SHR0302 and Steroid As First Line Therapy for Chronic GVHD (clinicaltrials.gov) - Oct 26, 2020 P1, N=30, Recruiting, Although the scale of this study is small, further research on large sample sizes is needed. Not yet recruiting --> Recruiting | Trial completion date: Nov 2021 --> May 2022 | Trial primary completion date: Nov 2021 --> Apr 2022
- |||||||||| AiTan (rivoceranib) / HLB Bio Group, AiRuiKa (camrelizumab) / Incyte
Journal: Anti-PD-1 plus a VEGFR2 Inhibitor Shows Promise in Cervical Cancer. (Pubmed Central) - Oct 26, 2020 Not yet recruiting --> Recruiting | Trial completion date: Nov 2021 --> May 2022 | Trial primary completion date: Nov 2021 --> Apr 2022 The PD-1 antibody camrelizumab plus the VEGFR2 inhibitor apatinib had efficacy in a phase II trial.
- |||||||||| AiTan (rivoceranib) / HLB Bio Group, AiRuiKa (camrelizumab) / HLB Bio Group
Trial completion, Trial completion date, Trial primary completion date, PD(L)-1 Biomarker, IO biomarker: A Trial of SHR-1210 (an Anti-PD-1 Antibody) in Combination With Apatinib in Patients With Advanced TNBC (clinicaltrials.gov) - Oct 22, 2020 P2, N=40, Completed, Our study identifies an alternate intracellular axis in DCs induced upon microtubule destabilization in which GEF-H1 promotes protective anti-tumor immunity. Active, not recruiting --> Completed | Trial completion date: Jun 2020 --> Sep 2020 | Trial primary completion date: Aug 2019 --> Dec 2019
- |||||||||| AiTan (rivoceranib) / HLB Bio Group, Opdivo (nivolumab) / Ono Pharma, BMS, AiRuiKa (camrelizumab) / Incyte
Clinical, P2 data, Journal: Anti-PD-1 antibody SHR-1210 plus apatinib for metastatic colorectal cancer: a prospective, single-arm, open-label, phase II trial. (Pubmed Central) - Oct 15, 2020 Grade 3 AEs were observed in nine patients (9/10, 90%), and the commonest was hypertension (30%). In conclusion, SHR-1210 combined with apatinib has failed to improve the efficacy of treatment of MSS mCRC, and the intolerable toxicity may be the leading cause.
- |||||||||| AiTan (rivoceranib) / HLB Bio Group, AiRuiKa (camrelizumab) / Incyte
[VIRTUAL] Anlyasis of Therapeutic effect and safty of PD-1 Inhibitors in Clinical treatment of Oral and Maxillofacial malignant tumors () - Oct 14, 2020 - Abstract #SITC2020SITC_1217; Among the 33 patients, 5 patients had immune-related adverse reactions (15.2%), including 2 cases of skin rash, 1 case of skin capillary hyperplasia and 2 cases of other adverse reactions. Conclusions The patients with Oral malignant tumor treated with PD-1 inhibitor Camrelizumab injection combined with targeted drug apatinib or postoperative adjuvant therapy can effectively control tumor development, improve the survival of patients, and help to improve the stability of postoperative efficacy.
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