- |||||||||| AiTan (rivoceranib) / HLB Bio Group, AiRuiKa (camrelizumab) / HLB Bio Group
P2 data, Journal, Combination therapy, Metastases: Efficacy and safety of camrelizumab, apatinib, and capecitabine combination therapy in advanced biliary tract cancer: a phase 2, nonrandomized, prospective study. (Pubmed Central) - Nov 13, 2024 P2 Even after complete excision, Rbr+ resection leads to a higher rate of local recurrence in patients with Br-ESCC. In this trial, the combination of camrelizumab, apatinib, and capecitabine showed promising antitumor activity and manageable toxicity in patients with advanced BTC, especially in the first-line setting.
- |||||||||| AiSuDa (ivarmacitinib) / Jiangsu Hengrui Pharma, Arcutis
Trial completion, Enrollment change, Trial completion date, Trial primary completion date: SHR0302 and Steroid As First Line Therapy for Chronic GVHD (clinicaltrials.gov) - Nov 13, 2024 P1, N=28, Completed, In this trial, the combination of camrelizumab, apatinib, and capecitabine showed promising antitumor activity and manageable toxicity in patients with advanced BTC, especially in the first-line setting. Recruiting --> Completed | N=73 --> 28 | Trial completion date: Jul 2024 --> Oct 2024 | Trial primary completion date: Jul 2024 --> Sep 2024
- |||||||||| AiTan (rivoceranib) / HLB Bio Group
Enrollment change, Trial completion date, Trial initiation date, Trial withdrawal, Trial primary completion date: A Phase II Study of Rivoceranib for Patients With Recurrent or Metastatic Olfactory Neuroblastoma (clinicaltrials.gov) - Nov 12, 2024 P2, N=0, Withdrawn, Not yet recruiting --> Recruiting N=16 --> 0 | Trial completion date: Nov 2028 --> Nov 2024 | Initiation date: Apr 2025 --> Nov 2024 | Not yet recruiting --> Withdrawn | Trial primary completion date: Nov 2026 --> Nov 2024
- |||||||||| Hengqu (hetrombopag) / Jiangsu Hengrui Pharma
Trial completion, Trial completion date, Trial primary completion date: Hetrombopag or Placebo in Treatment-Naive Severe Aplastic Anemia (clinicaltrials.gov) - Nov 7, 2024 P3, N=240, Completed, Active, not recruiting --> Completed Active, not recruiting --> Completed | Trial completion date: Dec 2024 --> Jul 2024 | Trial primary completion date: Dec 2024 --> Jul 2024
- |||||||||| Tevimbra (tislelizumab-jsgr) / BeOne Medicines, Keytruda (pembrolizumab) / Merck (MSD), AiRuiKa (camrelizumab) / HLB Bio Group
Enrollment open, Trial initiation date, Checkpoint inhibition, IO biomarker: ICI Rechallenge for Advanced NSCLC With Long-Term Response to First-Line ICI (clinicaltrials.gov) - Nov 6, 2024 P2, N=27, Recruiting, Active, not recruiting --> Completed | Trial completion date: Dec 2024 --> Jul 2024 | Trial primary completion date: Dec 2024 --> Jul 2024 Not yet recruiting --> Recruiting | Initiation date: May 2024 --> Aug 2024
- |||||||||| recaticimab (SHR-1209) / Jiangsu Hengrui Pharma
Clinical, P3 data, Journal, Monotherapy: Recaticimab Monotherapy for Nonfamilial (Pubmed Central) - Nov 6, 2024 Not yet recruiting --> Recruiting | Initiation date: May 2024 --> Aug 2024 Recaticimab monotherapy yielded significant LDL-C reductions and showed comparable safety vs placebo in patients with nonfamilial hypercholesterolemia and mixed hyperlipemia at low-to-moderate ASCVD risk, even
- |||||||||| Efficacy of Targeted Agents and Immune Checkpoint Inhibitors in Patients with Malignant Histiocytosis (Halls G-H (San Diego Convention Center)) - Nov 6, 2024 - Abstract #ASH2024ASH_5999;
TAs included BRAF inhibitor (vemurafenib [1]), MEK inhibitors (binimetinib [1], cobimetinib [2], trametinib [2]) and others (dasatinib [1], pazopanib [1], pexidartinib [1]), while ICIs were exclusively pembrolizumab (5)...TAs included BRAF inhibitor only (vemurafenib [3], dabrafenib [3]), MEK inhibitor only (trametinib [5]), BRAF + MEK inhibitors (2), and others (apatinib, anlotimib, bevacizumab, daratumumab, dasatinib, imatinib, pazopanib, sorafenib, or combinations [9]), while ICIs included pembrolizumab (4), nivolumab (4), tislelizumab (1), and sintilimab (1)...Conclusion TAs and ICIs can be considered in the management of MH. The responses to ICI therapy may be associated with the degree of PDL1 expression
- |||||||||| Koselugo (selumetinib) / Merck (MSD), AstraZeneca, plinabulin (BPI 2358) / BeyondSpring
Plinabulin and Selumetinib Enhance M1 Macrophage Traits and Trigger Cell Death in AML (Halls G-H (San Diego Convention Center)) - Nov 6, 2024 - Abstract #ASH2024ASH_5292; Additionally, both drugs were associated with reduced mitochondrial membrane potential in leukemic blasts and AAMs, suggesting an impact on mitochondrial metabolism. In conclusion, we found that both BPI-2358 and AZD6244 exhibit potential in repolarizing M2-like TAMs towards an M1-like phenotype, and have cytotoxic activity in AAM and leukemic blasts thus representing a promising avenue for enhancing AML treatment strategies.
- |||||||||| Hengqu (hetrombopag) / Jiangsu Hengrui Pharma
Hetrombopag, an Emerging Iron-Chelating Agent, Alleviates Systemic Iron Overload (Halls G-H (San Diego Convention Center)) - Nov 6, 2024 - Abstract #ASH2024ASH_4776; Furthermore, compared with those in DFX-treated mice, immune response-related signalling pathways, especially those related to the inhibition of the response to type I interferon, were significantly enriched in HPAG-treated mice. Conclusion : HPAG is an emerging iron-chelating agent and a potential inhibitor of ferroptosis that alleviates tissue damage, haematopoietic stem cell injury, and immune abnormalities caused by systemic iron overload and provides an immunoregulatory function.
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