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Nathalie Adda

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Articles 21
Citations 1621
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Recent Articles
1.
Feld J, Lawitz E, Nguyen T, Lalezari J, Hassanein T, Martin P, et al.
Antivir Ther . 2022 Nov; 27(6):13596535221127848. PMID: 36382358
Background: Chronic hepatitis B (CHB) remains a major cause of morbidity and mortality. EDP-514 is a potent core inhibitor of hepatitis B virus (HBV) that reduces viral load reduction in...
2.
Marotta C, Ahmad A, Luo E, Oosterhaven J, van Marle S, Adda N
Clin Transl Sci . 2022 Nov; 16(2):338-351. PMID: 36369848
EDP-297 is a farnesoid X receptor agonist under development for treating nonalcoholic steatohepatitis. The pharmacokinetic (PK), pharmacodynamic (PD), food effect, and safety were evaluated in a single ascending dose (SAD)...
3.
Ahmad A, Adda N
Clin Transl Sci . 2022 Jun; 15(9):2146-2158. PMID: 35675500
EDP-305 is a farnesoid X receptor (FXR) agonist that selectively activates FXR and is a potential treatment for patients with nonalcoholic steatohepatitis (NASH) with liver fibrosis. Results from preclinical studies...
4.
Ahmad A, Eze K, Noulin N, Horvathova V, Murray B, Baillet M, et al.
N Engl J Med . 2022 Feb; 386(7):655-666. PMID: 35172056
Background: Respiratory syncytial virus (RSV) infection causes substantial morbidity and mortality among infants, older adults, and immunocompromised adults. EDP-938, a nonfusion replication inhibitor of RSV, acts by modulating the viral...
5.
Ratziu V, Rinella M, Neuschwander-Tetri B, Lawitz E, Denham D, Kayali Z, et al.
J Hepatol . 2021 Nov; 76(3):506-517. PMID: 34740705
Background & Aims: EDP-305 is an oral farnesoid X receptor (FXR) agonist under development for the treatment of non-alcoholic steatohepatitis (NASH). Herein, we aimed to assess the efficacy, safety and...
6.
Zoulim F, Fournier C, Habersetzer F, Sprinzl M, Pol S, Coffin C, et al.
Hum Vaccin Immunother . 2019 Aug; 16(2):388-399. PMID: 31373537
Treatment of chronic hepatitis B (CHB) typically requires life-long administration of drugs. Cohort and pre-clinical studies have established the link between a functional T-cell-mounted immunity and resolution of infection. TG1050...
7.
Flamm S, Muir A, Fried M, Reddy K, Nelson D, Bzowej N, et al.
J Clin Gastroenterol . 2014 May; 49(4):336-44. PMID: 24828357
Background: The phase 3 studies of telaprevir (T) in combination with peginterferon α-2a and ribavirin (PR) in treatment-naive genotype 1 chronic hepatitis C virus-infected patients (ADVANCE/ILLUMINATE) were not designed a...
8.
Picchio G, De Meyer S, Dierynck I, Ghys A, Gritz L, Kieffer T, et al.
J Clin Virol . 2014 Jan; 59(3):148-55. PMID: 24462470
Background: Telaprevir-based therapy is associated with rapid decline in HCV RNA, enabling the application of early futility rules. Objectives: To familiarize physicians with this paradigm, a comprehensive analysis of the...
9.
Sulkowski M, Sherman K, Dieterich D, Bsharat M, Mahnke L, Rockstroh J, et al.
Ann Intern Med . 2013 May; 159(2):86-96. PMID: 23685940
Background: Telaprevir (TVR) plus peginterferon-α2a (PEG-IFN-α2a) and ribavirin substantially increases treatment efficacy for genotype 1 chronic hepatitis C virus (HCV) infection versus PEG-IFN-α2a-ribavirin alone. Its safety and efficacy in patients...
10.
Sullivan J, De Meyer S, Bartels D, Dierynck I, Zhang E, Spanks J, et al.
Clin Infect Dis . 2013 Apr; 57(2):221-9. PMID: 23575197
Background: Telaprevir (TVR), a hepatitis C virus (HCV) NS3/4A protease inhibitor, has been approved to treat genotype 1 HCV. To understand the clinical impact of TVR-resistant variants, we analyzed samples...