- |||||||||| oxaliplatin / Generic mfg., AiRuiKa (camrelizumab) / Incyte, capecitabine / Generic mfg.
[VIRTUAL] Changes in immune function and prognosis in advanced perihilar cholangiocarcinoma patients treated with immunotherapy combined with different topical therapies (On-Demand) - Jul 21, 2020 - Abstract #ESMO2020ESMO_424; Cohort A: 125I particle stent + HAI + camrelizumab; Cohort B: 125I particle stent + camrelizumab; Cohort C: HAI + camrelizumab...HAI plan: HAI consisted of infusions of oxaliplatin 40 mg/ m2 for 2 hours, followed by 5-fluorouracil 800 mg/m2 for 22 hours on days 1∼3 every 3 weeks, a maximum of 6 cycles of HAI are applied for tumor control patients followed by maintenance with oral capecitabine until tumor progression...Secondary endpoints includes progress free survival (PFS), near-term outcome indicators (TBIL/DBIL/AST/ALT/ CEA/CA199 etc.), long-term outcome indicators (stent patency rate/ tumour response rate etc.), complications (fever/ bleeding/pain etc.), changes in immune-inflammatory cytokines (TNF-α/IL-1β/IL-6/ IL-8/CD4/CD8/IgA/IgG/IgM/complement C3 and C4), etc. Legal entity responsible for the study: The authors. Funding: Has not received any funding.
- |||||||||| AiRuiKa (camrelizumab) / Incyte, irinotecan / Generic mfg.
Clinical, P3 data, Clinical Trial,Phase III, Journal: Camrelizumab versus investigator's choice of chemotherapy as second-line therapy for advanced or metastatic oesophageal squamous cell carcinoma (ESCORT): a multicentre, randomised, open-label, phase 3 study. (Pubmed Central) - Jul 21, 2020 P3 Second-line camrelizumab significantly improved overall survival in patients with advanced or metastatic oesophageal squamous cell carcinoma compared with chemotherapy, with a manageable safety profile. It might represent a potential option of standard second-line treatment for patients with oesophageal squamous cell carcinoma in China.
- |||||||||| AiRuiKa (camrelizumab) / HLB Bio Group
Trial initiation date, Real-world evidence: RFA Plus Carrizumab vs Carrizumab Alone for HCC (clinicaltrials.gov) - Jul 7, 2020 P2, N=120, Recruiting, Camrelizumab showed antitumour activity in pretreated Chinese patients with advanced hepatocellular carcinoma, with manageable toxicities, and might represent a new treatment option for these patients. Initiation date: Jan 2020 --> Aug 2020
- |||||||||| AiRuiKa (camrelizumab) / HLB Bio Group
Trial completion date, Trial initiation date, Trial primary completion date: Carbon-Ion Radiotherapy Plus Camrelizumab for Locally Recurrent Nasopharyngeal Carcinoma (clinicaltrials.gov) - Jul 7, 2020 P2/3, N=180, Not yet recruiting, Initiation date: Jan 2020 --> Aug 2020 Trial completion date: May 2025 --> Sep 2025 | Initiation date: May 2020 --> Sep 2020 | Trial primary completion date: May 2024 --> Sep 2024
- |||||||||| Opdivo (nivolumab) / Ono Pharma, BMS, Cabometyx (cabozantinib tablet) / Takeda, Exelixis, Ipsen
Review, Journal: Emerging agents and regimens for hepatocellular carcinoma. (Pubmed Central) - Jun 28, 2020 The combination of an anti-PD-1 antibody and an anti-angiogenesis agent has shown more potent anti-tumor effects in early phase clinical trials and is now the hotspot in clinical studies. Furthermore, these agents are investigated in combination treatment with surgery or other loco-regional therapies in patients with early or intermediate-stage HCC.
- |||||||||| AiRuiKa (camrelizumab) / HLB Bio Group
Enrollment closed: SHR-1210 in Patients With Relapsed or Refractory Extranodal NK/T Cell Lymphoma (clinicaltrials.gov) - Jun 17, 2020 P2, N=97, Active, not recruiting, Recruiting --> Active, not recruiting | Trial completion date: Mar 2020 --> Dec 2020 | Trial primary completion date: Sep 2019 --> Jun 2020 Not yet recruiting --> Active, not recruiting
- |||||||||| luxeptinib (CG-806) / Aptose Biosci
Trial completion date, Trial primary completion date: A Study of CG-806 in Patients With Relapsed or Refractory CLL/SLL or Non-Hodgkin's Lymphomas (clinicaltrials.gov) - Jun 4, 2020 P1, N=130, Recruiting, Decitabine plus camrelizumab may reverse resistance to PD-1 inhibitors in patients with relapsed/refractory cHL. Trial completion date: Dec 2020 --> May 2022 | Trial primary completion date: Nov 2020 --> Dec 2021
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