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Profil bibliographique

Grant Langdon

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

28Publications signalées
1008Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

HIV/AIDS drug development and treatmentTuberculosis Research and EpidemiologyPharmacogenetics and Drug MetabolismAntibiotics Pharmacokinetics and EfficacyMalaria Research and Control

Les publications récentes

Accès ouvert 2025 article OpenAlex

Anti‐Neuroinflammatory and Anti‐Inflammatory Effects of the NLRP3 Inhibitor NT ‐0796 in Subjects with Parkinson's Disease

Nicholas P. Clarke, Peter Thornton, Valérie Reader, Nicola A. Lindsay et autres

BACKGROUND: Inhibition of Nod-like receptor protein 3 (NLRP3) inflammasome within the central nervous system (CNS) is a promising therapeutic target for the treatment of Parkinson's disease (PD). OBJECTIVES: This phase 1b open-label study was conducted in elderly healthy volunteers (HV) and PD …

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34 citations Movement Disorders
Accès ouvert 2024 article OpenAlex

Population Pharmacokinetic and Pharmacokinetic/Pharmacodynamic Analyses of Pegcetacoplan in Patients with Paroxysmal Nocturnal Hemoglobinuria

Ryan L. Crass, Brandon A. Smith, Sven Adriaens, Sunny Hong Chapel et autres

Paroxysmal nocturnal hemoglobinuria is a rare blood disorder characterized by life-threatening hemolysis and thrombosis. Complement C5 inhibitor therapy improves symptoms and life prognosis; however, it can result in insufficient hemolysis control, with residual intravascular hemolysis and extravascular hemolysis in some patients. Pegcetacoplan, …

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4 citations Drugs in R&D
Accès ouvert 2021 article OpenAlex

Chemoprotective Antimalarial Activity of P218 against Plasmodium falciparum: A Randomized, Placebo-Controlled Volunteer Infection Study

Mohamed Farouk Chughlay, Myriam El Gaaloul, Cristina Donini, Brice Campo et autres

P218 is a highly selective dihydrofolate reductase inhibitor with potent in vitro activity against pyrimethamine-resistant Plasmodium falciparum. This single-center, randomized, double-blind, placebo-controlled phase Ib study evaluated P218 safety, pharmacokinetics, and chemoprotective efficacy in a P. falciparum sporozoite (PfSPZ) volunteer infection study (VIS). …

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32 citations American Journal of Tropical Medicine and Hygiene
Accès ouvert 2020 article OpenAlex

Phase 2 multiple-dose study of an FcRn inhibitor, rozanolixizumab, in patients with primary immune thrombocytopenia

Tadeusz Robak, Maciej Kaźmierczak, Isidro Jarque, Vasile Musteata et autres

Primary immune thrombocytopenia (ITP) is a predominantly immunoglobulin G (IgG)-autoantibody-mediated disease characterized by isolated thrombocytopenia. Rozanolixizumab, a subcutaneously infused humanized monoclonal anti-neonatal Fc receptor (FcRn) antibody, reduced serum IgG in healthy volunteers. In this phase 2, multicenter, open-label study, patients with persistent/chronic …

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112 citations Blood Advances
Accès ouvert 2020 article OpenAlex

First‐in‐human clinical trial to assess the safety, tolerability and pharmacokinetics of P218, a novel candidate for malaria chemoprotection

Mohamed Farouk Chughlay, Emilie Rossignol, Cristina Donini, Myriam El Gaaloul et autres

Aims This first‐in‐human clinical trial of P218, a novel dihydrofolate reductase inhibitor antimalarial candidate, assessed safety, tolerability, pharmacokinetics and food effects in healthy subjects. Methods The study consisted of two parts. Part A was a double‐blind, randomized, placebo‐controlled, parallel group, ascending dose …

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42 citations British Journal of Clinical Pharmacology
Accès ouvert 2020 article OpenAlex

Safety, Tolerability, Pharmacokinetics, and Antimalarial Activity of the Novel Plasmodium Phosphatidylinositol 4-Kinase Inhibitor MMV390048 in Healthy Volunteers

Phumla Sinxadi, Cristina Donini, Hilary Johnstone, Grant Langdon et autres

induced blood-stage malaria (IBSM) model. Due to the high pharmacokinetic variability with the powder-in-bottle formulation used in both of these studies, a third study was undertaken to select a tablet formulation of MMV390048 to take forward into future studies. MMV390048 was generally …

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62 citations Antimicrobial Agents and Chemotherapy
Accès ouvert 2019 conference-abstract OpenAlex

Rozanolixizumab, an Anti-FcRn Antibody: Final Results from a Phase II, Multiple-Dose Study in Patients with Primary Immune Thrombocytopenia

Tadeusz Robak, Maciej Kaźmierczak, Isidro Jarque, Vasile Musteata et autres

Introduction Rozanolixizumab targets the human neonatal Fc receptor (FcRn). By blocking IgG recycling, this first-in-class subcutaneously (SC) infused monoclonal antibody aims to improve the course of immunoglobulin G (IgG)-mediated autoimmune diseases by reducing pathogenic autoantibody levels. We report the completed Phase II, …

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5 citations Blood
2017 article OpenAlex

The FcRn inhibitor rozanolixizumab reduces human serum IgG concentration: A randomized phase 1 study

Peter C. Kiessling, Rocío Lledó‐García, Shikiko Watanabe, Grant Langdon et autres

= 1)]. Rozanolixizumab pharmacokinetics demonstrated nonlinear increases with dose. There were sustained dose-dependent reductions in serum IgG concentrations (IV and SC rozanolixizumab). These data provide clinical evidence for the therapeutic potential of rozanolixizumab.

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205 citations Science Translational Medicine
2015 conference-abstract OpenAlex

Systemic inhibition of p38 MAPK improves lung function and inflammatory markers in moderate-severe COPD

Spencer I. Danto, Grant Langdon, Negin Shojaee, Jared L. Christensen et autres

COPD is characterized by inflammation and lung function decline. p38 MAPK inhibition may be an anti-inflammatory therapeutic approach to COPD. The efficacy and safety of PH-797804 (PH), a potent, selective oral p38 inhibitor, was tested in three studies including patients with GOLD …

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1 citation
2013 conference-abstract OpenAlex

A phase II, randomised, placebo controlled trial of 12 weeks treatment with an oral p38 inhibitor in patients with COPD on a background of ICS/LABA

Robert Fogel, Kathleen M. Shields, Jared L. Christensen, Jakob Ribbing et autres

Despite the recognized role of pulmonary inflammation in the pathogenesis of the disease, anti-inflammatory drugs have demonstrated only limited efficacy in COPD. Inhibitors of the p38 MAP kinase may have an important role in treating inflammation in COPD. Here we extend previous …

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5 citations European Respiratory Journal
2013 article OpenAlex

Pharmacokinetic Interactions between Lersivirine and Zidovudine, Tenofovir Disoproxil Fumarate/ Emtricitabine and Abacavir/Lamivudine

Manoli Vourvahis, John D. Davis, Grant Langdon, Gary R. Layton et autres

BACKGROUND: To investigate pharmacokinetic interactions associated with coadministration of lersivirine with zidovudine, tenofovir disoproxil fumarate (DF)/emtricitabine (Truvada(®)) or abacavir/lamivudine (Epzicom(®)/Kivexa(®)). METHODS: Three Phase I, open, crossover studies with two (studies 1 and 3) or three (study 2) treatment periods were conducted in …

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4 citations Antiviral Therapy
2012 article OpenAlex

The Pharmacokinetics of Lersivirine (UK-453,061) and HIV-1 Protease Inhibitor Coadministration in Healthy Subjects

Manoli Vourvahis, Grant Langdon, Gary R. Layton, Robert R. LaBadie et autres

OBJECTIVE: Lersivirine (UK-453,061) is a next-generation nonnucleoside reverse transcriptase inhibitor, active against wild-type HIV-1 and several nonnucleoside reverse transcriptase inhibitor-resistant strains. Four studies evaluated the pharmacokinetic (PK) interactions between lersivirine and various HIV-1 protease inhibitors. METHODS: Four phase I trials were conducted …

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4 citations JAIDS Journal of Acquired Immune Deficiency Syndromes

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