ALLMedicine™ Cold Agglutinin Disease Center
Research & Reviews 104 results
https://doi.org/10.1111/ijlh.13860
International Journal of Laboratory Hematology; Chang SH
May 17th, 2022 - The author report an interesting case of relapsed diffuse large B-cell lymphoma (DLBCL) with bone marrow (BM) and peripheral blood (PB) involvement after prior cold agglutinin disease (CAD). A minority of patients with DLBCL present with CAD, and ...
https://clinicaltrials.gov/ct2/show/NCT04269551
May 2nd, 2022 - Up to 23 weeks (screening period up to 8 weeks, treatment period 15 weeks)
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9058691
BMJ Case Reports; Dawudi Y, Federici L et. al.
Apr 30th, 2022 - Impaired immune response with uncontrolled inflammation and various immunological disorders have been reported during SARS-CoV-2 infection. Here, we report a case of cold agglutinin disease occurring during a severe coronavirus disease 2019 (COVID...
https://clinicaltrials.gov/ct2/show/NCT03347396
Apr 25th, 2022 - The purpose of Part A is to determine whether sutimlimab administration results in a greater than or equal to (>=) 2 gram per deciliter (g/dL) increase in hemoglobin (Hgb) levels or increases Hgb to >= 12 g/dL and obviates the need for blood trans...
https://doi.org/10.1007/s40265-022-01711-5 10.2991/chi.k.200706.001 10.2147/JBM.S177621 10.1186/s12979-020-00208-7 10.3390/jcm9123859 10.1002/cpt.1111 10.1056/NEJMoa2027760 10.1182/blood-2021-148066 10.1182/blood-2020-140335 10.1182/blood-2020-139738 10.3324/haematol.2021.279812 10.1002/ajh.26409 10.1182/blood-2021-147759 10.1186/s13023-016-0494-z 10.1097/TP.0000000000001804 10.1182/blood-2018-06-856930 10.1182/bloodadvances.2019001321 10.1111/ajt.14528
Drugs Dhillon S
Apr 13th, 2022 - Sutimlimab (sutimlimab-jome; ENJAYMO™) is a humanized monoclonal antibody developed by Sanofi for the treatment of cold agglutinin disease (CAD). Sutimlimab is an immunoglobulin G, subclass 4 (IgG4) monoclonal antibody that inhibits the classical ...
Drugs 1 results see all →
Clinicaltrials.gov 3 results
https://clinicaltrials.gov/ct2/show/NCT04269551
May 2nd, 2022 - Up to 23 weeks (screening period up to 8 weeks, treatment period 15 weeks)
https://clinicaltrials.gov/ct2/show/NCT03347396
Apr 25th, 2022 - The purpose of Part A is to determine whether sutimlimab administration results in a greater than or equal to (>=) 2 gram per deciliter (g/dL) increase in hemoglobin (Hgb) levels or increases Hgb to >= 12 g/dL and obviates the need for blood trans...
https://clinicaltrials.gov/ct2/show/NCT01696474
Oct 27th, 2017 - Based on its activity in MM, single agent Bortezomib was tested in phase II trials in lymphoplasmacytic lymphoma, the disorder most frequently associated with CAD, and achieved 40-80% responses. These striking clinical responses indicate that prot...
News 11 results
https://www.onclive.com/view/experimental-agents-for-itp
Feb 23rd, 2022 - Craig Kessler, MD: Sutimlimab is a humanized monoclonal antibody that selectively inhibits activation of the complement pathway by binding to complement 1S. This drug, which is not approved, will be marketed by Sanofi. It was originally developed ...
https://www.medpagetoday.com/hematologyoncology/othercancers/97125
Feb 10th, 2022 - A 30-year-old investigational drug could get another look as a potential cancer therapy as a result of the growing emphasis on precision medicine. (VCU Health, Molecular Cancer Therapeutics) The Centers for Medicare & Medicaid Services expanded el...
https://www.medscape.com/viewarticle/967966
Feb 7th, 2022 - A new drug has become the first and only treatment for people with cold agglutinin disease (CAD) that is approved by the US Food and Drug Administration (FDA). CAD is a rare autoimmune hemolytic anemia, affecting about 5000 people in the United St...
https://www.medscape.com/viewarticle/959368
Nov 18th, 2021 - Cold agglutinin disease (CAD) is a rare, complement-dependent, classical pathway–mediated immune hemolytic disease, accounting for up to 25% of autoimmune hemolytic anemia. Whereas the incidence of CAD is rare, the disease burden is frequently hig...
https://www.reuters.com/article/us-sanofi-products/sanofi-gets-priority-u-s-fda-review-for-sutimlimab-product-idUSKBN22Q0JI
May 14th, 2020 - FILE PHOTO: The logo of Sanofi is seen at the company's headquarters in Paris, France, April 24, 2020. REUTERS/Charles Platiau PARIS (Reuters) - French healthcare company Sanofi said on Thursday that the U.S. Food & Drug Administration (FDA) regul...