CD Protein Inhibitors 

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  • ||||||||||  Keytruda (pembrolizumab) / Merck (MSD)
    Trial completion date, Trial primary completion date, Surgery:  Study of Combined Decompressive Spine Radiosurgery and Pembrolizumab (clinicaltrials.gov) -  Sep 24, 2024   
    P1,  N=10, Recruiting, 
    Trial completion date: Sep 2024 --> Dec 2024 | Trial primary completion date: Sep 2024 --> Dec 2024
  • ||||||||||  Opdivo (nivolumab) / BMS, Yervoy (ipilimumab) / BMS
    Journal, BRCA Biomarker, PD(L)-1 Biomarker, IO biomarker:  Malignant pleural mesothelioma: The disdained member of thoracic oncology! (Pubmed Central) -  Sep 23, 2024   
    This review article provides an overview of epidemiology, etiology, clinical manifestations, diagnostic approaches (including immunohistochemical and genetic markers), staging, and multidisciplinary approaches to current treatment for malignant pleural mesothelioma using surgery, chemotherapy, immunotherapy, and radiotherapy. It also sheds light on some recent studies (EMPHACIS, CALGB30901, Checkmate-743, etc.) that have led to significant developments in recent years with clinically meaningful results.
  • ||||||||||  Darzalex (daratumumab) / J&J
    Journal:  Response to daratumumab-retreatment in patients with multiple myeloma. (Pubmed Central) -  Sep 23, 2024   
    Our findings suggest that well-selected daratumumab-exposed MM patients may show rewarding responses to daratumumab retreatment, the more with alternating antimyeloma combinations, initial good response and CD38-antibody-treatment pauses, thereby proving CD38-antibody-retreatment as feasible, effective and non-toxic. Confirmatory studies are required to further validate our results.
  • ||||||||||  Review, Journal:  Evolving Horizons in Pediatric Leukemia: Novel Insights, Challenges, and the Journey Ahead. (Pubmed Central) -  Sep 23, 2024   
    This review also discusses the long-term outcomes among pediatric leukemia survivors, focusing on late-onset side effects associated with treatments such as chemotherapy and bone marrow transplantation, encompassing secondary malignancies, organ dysfunction, and neurocognitive impacts. Ongoing research and clinical trials are crucial to refine these therapies, enhance their efficacy, and reduce adverse effects, ultimately improving young patients' survival and quality of life.
  • ||||||||||  Venclexta (venetoclax) / Roche, AbbVie, Imbruvica (ibrutinib) / AbbVie, J&J
    Journal, IO biomarker:  Paraneoplastic myelitis associated with Waldenstr (Pubmed Central) -  Sep 23, 2024   
    However, he subsequently relapsed and symptomatically worsened while on rituximab therapy...Our observation of sustained disease response in this patient may support a role for concurrent BTK and BCL2 inhibition in paraneoplastic myelitis associated with B-cell lymphoproliferative disorders. However, this observation needs to be validated in larger cohort studies and potentially in clinical trials if further data are supportive.
  • ||||||||||  Ibrance (palbociclib) / Pfizer
    PK/PD data, Journal, Metastases:  Exploring pharmacokinetic variability of palbociclib in HR+/HER2- metastatic breast cancer: a focus on age, renal function, and drug-gene interactions. (Pubmed Central) -  Sep 23, 2024   
    Furthermore, exploring the drug-drug-gene interactions between inhibitors of CYP3A and P-glycoprotein with their respective genetic variants revealed two patient groups with statistically different percentage deviations (p = 0.0075, p = 0.0012, and p = 0.0191, respectively). These results could help address cases where pharmacokinetic covariates or subclinical conditions impair palbociclib adherence or response, aiming to offer tailored dosing strategies or monitoring for individual patients.
  • ||||||||||  Review, Journal, PD(L)-1 Biomarker, IO biomarker:  Immunotherapy for hepatocellular carcinoma. (Pubmed Central) -  Sep 23, 2024   
    Combination therapy with either atezolizumab (anti-PD-L1) and bevacizumab (anti-VEGF) or durvalumab (anti-PD-L1) and tremelimumab (anti-CTLA-4) is now recognised as standard of care for advanced HCC...Herein, we review the current understanding of the immune landscape in which HCC develops and the evidence for ICI-based therapeutic strategies in HCC. Additionally, we describe the state of biomarker development and novel immunotherapy approaches in HCC which have progressed beyond the pre-clinical stage and into early-phase trials.
  • ||||||||||  Kymriah (tisagenlecleucel-T) / Novartis, Yescarta (axicabtagene ciloleucel) / Gilead
    Retrospective data, Journal:  Comparison of the Efficacy and Safety of Axi-Cel and Tisa-Cel Based on Meta-Analysis. (Pubmed Central) -  Sep 23, 2024   
    CAR T-cell therapy is an effective treatment option for relapsed/refractory B-cell lymphoma. Axi-cel has better ORR and survival advantages compared with tisa-cel; however, axi-cel has higher incidence rates of CRS and ICANS compared with tisa-cel.
  • ||||||||||  mRNA-4157 / Merck (MSD), Moderna, BNT111 / BioNTech
    Review, Journal:  mRNA vaccines: a new era in vaccine development. (Pubmed Central) -  Sep 23, 2024   
    Overall, mRNA cancer vaccines represent a cutting-edge therapeutic approach that holds the promise of transforming cancer treatment. As research progresses, addressing challenges and refining manufacturing processes will be crucial in advancing these vaccines from clinical trials to mainstream oncology practice, offering new hope for patients in the fight against cancer.
  • ||||||||||  Venclexta (venetoclax) / Roche, AbbVie, Rituxan (rituximab) / Roche, Imbruvica (ibrutinib) / AbbVie, J&J
    Trial termination:  A Study of ABT-199 Plus Ibrutinib and Rituximab in Patients With Relapsed/Refractory Diffuse Large B-cell Lymphoma (clinicaltrials.gov) -  Sep 23, 2024   
    P1,  N=10, Terminated, 
    In conclusion, we developed a feasible risk score model based on IPS-related genes for cervical cancer prognosis and identified potential drugs for different cervical cancer subtypes. Active, not recruiting --> Terminated; Lack of enrollment
  • ||||||||||  Keytruda (pembrolizumab) / Merck (MSD)
    Trial completion, Trial completion date, Trial primary completion date:  Assess the Efficacy of Pembrolizumab Plus Radiotherapy or Ablation in Metastatic Colorectal Cancer Patients (clinicaltrials.gov) -  Sep 23, 2024   
    P2,  N=34, Completed, 
    Recruiting --> Active, not recruiting | Trial completion date: Sep 2025 --> Dec 2025 | Trial primary completion date: Mar 2025 --> Dec 2024 Active, not recruiting --> Completed | Trial completion date: Apr 2025 --> Sep 2024 | Trial primary completion date: Apr 2025 --> Sep 2024
  • ||||||||||  SAR442257 / Sanofi
    Journal, IO biomarker, Trispecific:  A CD38/CD3xCD28 trispecific T-cell engager as a potentially active agent in multiple myeloma patients relapsed and/or refractory to anti-CD38 monoclonal antibodies. (Pubmed Central) -  Sep 23, 2024   
    While complete CD38 loss is not observed upon relapses after treatment with anti-CD38 monoclonal antibodies (mAb), there is downregulation of surface CD38 expression and decreased number and function of NK cells, which renders these patients resistant to retreatment with anti-CD38 mAb. Here, we provide preclinical evidence that RRMM patients previously exposed to anti-CD38 mAb could benefit from T-cell-based immunotherapy that depend less on CD38 antigen density and NK-cell activity, such as the novel CD38/CD3xCD28 trispecific T-cell engager, SAR442257.
  • ||||||||||  TG01 vaccine / Circio Holding, balstilimab (AGEN2034) / Agenus
    Enrollment closed:  TESLA: Tg01 Vaccine / Qs-21 Stimulon (clinicaltrials.gov) -  Sep 23, 2024   
    P2,  N=24, Active, not recruiting, 
    Suspended --> Recruiting Recruiting --> Active, not recruiting
  • ||||||||||  Venclexta (venetoclax) / Roche, AbbVie, Gazyva (obinutuzumab) / Roche, Biogen, Calquence (acalabrutinib) / AstraZeneca
    Trial completion date, Trial primary completion date, Combination therapy:  Acalabrutinib in Combination with Venetoclax or Obinutuzumab for the Treatment of Treatment-naive Chronic Lymphocytic Leukemia (clinicaltrials.gov) -  Sep 23, 2024   
    P2,  N=52, Recruiting, 
    Trial completion date: Mar 2025 --> Dec 2026 | Trial primary completion date: Aug 2024 --> Jul 2025 Trial completion date: Dec 2024 --> Dec 2025 | Trial primary completion date: Dec 2024 --> Dec 2025