- |||||||||| Lamprene (clofazimine) / Novartis, Humira (adalimumab) / Eisai, AbbVie
Review, Journal: Medication-Induced Repigmentation of Gray Hair: A Systematic Review. (Pubmed Central) - Feb 6, 2020 There is also low-quality evidence that some vitamin B complex supplementation can promote gray hair darkening. While these compounds are not currently indicated for the treatment of gray hair, their mechanisms shed light on targets for future medications for hair repigmentation.
- |||||||||| Remicade (infliximab) / J&J, NN1213 / Novo Nordisk, Humira (adalimumab) / AbbVie
Trial completion date: SUSI-CS: Stavanger IBD Study - Cross Sectional (clinicaltrials.gov) - Feb 5, 2020 P=N/A, N=210, Active, not recruiting, While these compounds are not currently indicated for the treatment of gray hair, their mechanisms shed light on targets for future medications for hair repigmentation. Trial completion date: Nov 2020 --> Dec 2021
- |||||||||| Humira (adalimumab) / AbbVie
Enrollment closed, Enrollment change, Trial completion date, Trial primary completion date: Long-term Safety and Efficacy Study of Adalimumab in Pediatric Subjects With Ulcerative Colitis (clinicaltrials.gov) - Feb 5, 2020 P3, N=59, Active, not recruiting, Trial completion date: Nov 2020 --> Dec 2021 Enrolling by invitation --> Active, not recruiting | N=93 --> 59 | Trial completion date: Mar 2026 --> May 2025 | Trial primary completion date: May 2023 --> Mar 2025
- |||||||||| Humira (adalimumab) / AbbVie
Trial completion date, Trial primary completion date, HEOR: Rheumatoid Arthritis Satisfaction Outcome Research (clinicaltrials.gov) - Feb 5, 2020 P=N/A, N=840, Recruiting, Enrolling by invitation --> Active, not recruiting | N=93 --> 59 | Trial completion date: Mar 2026 --> May 2025 | Trial primary completion date: May 2023 --> Mar 2025 Trial completion date: Dec 2019 --> Mar 2020 | Trial primary completion date: Dec 2019 --> Mar 2020
- |||||||||| Humira (adalimumab) / Eisai, AbbVie
Steroid-sparing agents for the treatment of inflammation in complicated neurocysticercosis () - Feb 3, 2020 - Abstract #AAN2020AAN_4949; We describe 3 cases of persistent neurocysticercosis-associated inflammation that highlight both the efficacy and complications of SSAs use in neurocysticercosis. Our series emphasizes the need for further study on the use of SSAs in the treatment of neurocysticercosis-related inflammation.
- |||||||||| Humira (adalimumab) / Eisai, AbbVie
Journal: Niemann-Pick disease type C presenting as very early onset inflammatory bowel disease. (Pubmed Central) - Feb 1, 2020 He did not have any typical neurological symptoms at the time of his diagnosis. He is currently doing well on biweekly adalimumab injections for his Crohn's disease and biweekly intrathecal injections of 2-hydroxypropyl-β-cyclodextrin (VTS-270) for the NPC.
- |||||||||| Remicade (infliximab) / Mitsubishi Tanabe, J&J, Enbrel (etanercept) / Pfizer, Amgen, Humira (adalimumab) / Eisai, AbbVie
Clinical, Journal: Risk of tuberculosis in patients with immune-mediated diseases on biological therapies: a population-based study in a tuberculosis endemic region. (Pubmed Central) - Jan 31, 2020 The risk of TB with TNF inhibitor was higher than with a non-TNF biologic (hazard ratio 4.34; 95% CI 1.31-14.39), while the risk of infliximab was higher than etanercept and adalimumab (hazard ratio: 4.10 and 2.08, respectively). The risk of TB is much higher in patients with immune-mediated diseases on biological therapy compared with the general population, and infliximab is associated with the highest risk of TB among the biologics analysed.
- |||||||||| Journal: Inflammatory bowel disease and targeted oral anti-TNFα therapy. (Pubmed Central) - Jan 31, 2020
Several oral anti-TNFα agents have been investigated with success but are not yet in general clinical use. This partially reflects the fact that the oral administration of antibodies has many barriers including the harsh environment of the GI tract and the presence of enzymes including pepsin, trypsin and chymotrypsin in the intestine which provide significant challenges to targeted oral therapy.
- |||||||||| Humira (adalimumab) / Eisai, AbbVie
Clinical, Journal: Pulmonary aspergillosis in a Crohn's disease patient receiving adalimumab and steroid therapy. (Pubmed Central) - Jan 30, 2020 This partially reflects the fact that the oral administration of antibodies has many barriers including the harsh environment of the GI tract and the presence of enzymes including pepsin, trypsin and chymotrypsin in the intestine which provide significant challenges to targeted oral therapy. No abstract available
- |||||||||| Stelara (ustekinumab) / J&J, Humira (adalimumab) / Eisai, AbbVie
Clinical, Journal: Biologics exposure during pregnancy and breastfeeding in a psoriasis patient. (Pubmed Central) - Jan 28, 2020 There are few data available on biologics treatment safety during pregnancy and breastfeeding, especially regarding ustekinumab. We report our positive experience with the aim of increasing case notifications, facilitate meta-analysis and eventual consensus recommendations regarding the use of biologics in special population.
- |||||||||| Humira (adalimumab) / Eisai, AbbVie
Journal: Adalimumab (Pubmed Central) - Jan 28, 2020 We report our positive experience with the aim of increasing case notifications, facilitate meta-analysis and eventual consensus recommendations regarding the use of biologics in special population. No abstract available
- |||||||||| Remicade (infliximab) / Mitsubishi Tanabe, J&J, Entyvio (vedolizumab) / Takeda, Humira (adalimumab) / Eisai, AbbVie
VEDOLIZUMAB - PERIOPERATIVE INFECTION RATES IN PATIENTS WITH IBD () - Jan 28, 2020 - Abstract #DDW2020DDW_3134; Our findings suggested that VDZ is safe to use during the perioperative period and it does not increase perioperative risk of infection. We recommend further investigations with prospective study and larger population coverage to solidify our findings.
- |||||||||| Remicade (infliximab) / Mitsubishi Tanabe, J&J, Simponi (golimumab) / Merck (MSD), Mitsubishi Tanabe, J&J, Humira (adalimumab) / Eisai, AbbVie
TRANSMURAL HEALING IN PATIENTS WITH CROHN’S DISEASE TREATED WITH ANTI-TNF THERAPY () - Jan 28, 2020 - Abstract #DDW2020DDW_3129; Conclusion Transmural healing, which is associated with better outcomes in CD, can be achieved in more than half of patients with CD. The best time to assess transmural healing was between 6 to 8 months after starting anti-TNF therapy.
- |||||||||| Remicade (infliximab) / Mitsubishi Tanabe, J&J, Simponi (golimumab) / Merck (MSD), Mitsubishi Tanabe, J&J, Humira (adalimumab) / Eisai, AbbVie
HIGH RATE OF LOSS OF RESPONSE POST DE-ESCALATION DESPITE PROLONGED EXPOSURE TO COMBINATION THERAPY () - Jan 28, 2020 - Abstract #DDW2020DDW_3120; Adequate serum concentration of the TNF inhibitor prior to deescalation was not protective against LOR. Any decision to de-escalate must be carefully considered and patients advised of the possible consequences
- |||||||||| EVALUATION OF BIOLOGIC TREATMENT PATTERNS AMONG CROHN’S DISEASE PATIENTS USING THREE LARGE UNITED STATES CLAIMS DATABASES () - Jan 28, 2020 - Abstract #DDW2020DDW_3119;
Introduction: Real-world evidence on treatment patterns among Crohn’s disease (CD) patients using biologics remains limited, particularly among ustekinumab (UST) patients...Patients (aged 18-64 years) were required to have ≥1 claim for CD and ≥1 claim for biologics (UST, vedolizumab [VDZ], infliximab [IFX], certolizumab pegol [CZP], or adalimumab [ADA]) during the identification period (IQVIA: 09/26/16-12/31/17; MarketScan: 09/26/16-09/30/17; Optum: 09/26/16-03/31/18)... Among CD patients, unadjusted persistence was numerically higher in the UST cohort with consistent trends in the bio-naïve and bio-experienced subsets.
- |||||||||| Remicade (infliximab) / Mitsubishi Tanabe, J&J, Enbrel (etanercept) / Pfizer, Amgen, Humira (adalimumab) / Eisai, AbbVie
ANTI-TUMOR NECROSIS FACTOR THERAPY AND EOSINOPHILIC ESOPHAGITIS: IS THERE A CONNECTION? () - Jan 28, 2020 - Abstract #DDW2020DDW_2933; The initiation of an anti-TNF in patients with IMD was associated with an increased occurrence of EoE in our population. The underlying pathophysiologic mechanism of this increased risk of anti-TNF therapy requires further investigation.
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