Borje Darpo
Borje Darpo has a total of 31 co-authors. Here are the top co-authors by number of shared publications:
- Andreas G. Moraitis
Dipartimento di Medicina Clinica e Chirurgia, Sezione di Endocrinologia, Università Federico II di Napoli, Naples, Italy
1 shared publication - Ani Amar
ELEM Biotech, Barcelona, Spain
1 shared publication - Antonio Stigliano
Endocrinology, Department of Clinical and Molecular Medicine, Sant’Andrea University Hospital, Sapienza University of Rome , 00189 Rome
1 shared publication - Austin L. Hand
Corcept Therapeutics Incorporated, Menlo Park, CA, USA
1 shared publication Barry Byrne
Institute for Child Health Policy University of Florida Gainesville Florida USA
1 shared publication- Cary N. Mariash
Division of Endocrinology, Indiana University School of Medicine, Indianapolis, IN, USA
1 shared publication
Latest Publications
- Open Access
- 22 March 2026
- Published by Wiley in Clinical Pharmacology in Drug Development
- Vol. 15 (3) , e70047
Thorough QT Study on the Effect of Therapeutic and Supratherapeutic Dosing of Givinostat in Healthy Volunteers
Givinostat is a class I/II histone deacetylase inhibitor indicated for Duchenne muscular dystrophy (DMD). The study evaluated the effect of therapeutic and supratherapeutic givinostat doses on the QT/QTc interval. Healthy volunteers received each treatment—givinostat hydrochloride monohydrate oral suspension as a therapeutic (100 mg) or supratherapeutic (300 mg) dose, placebo oral suspension, or moxifloxacin oral tablet (positive control, 400 mg)—according to a block randomization scheme. Cardiodynamic assessments were paired with pharmacokinetic samples. A small, clinically non‐relevant effect on mean placebo‐corrected, change‐from‐baseline QTcF (∆∆QTcF) of 5.5 ms was seen after givinostat 100‐mg dose. Clinically relevant QTc prolongation was observed with the supratherapeutic dose, with a mild ∆∆QTcF increase of 13.6 ms. A delay of ≈3 h between T max and the largest effect on the QTc interval was seen for both doses. In the concentration‐QTc analysis, an E max model captured the data better than the prespecified linear model and showed that an effect on ∆∆QTcF exceeding 10 ms could be excluded within the full range of observed givinostat concentrations in this study and up to ≈745 ng/mL. Givinostat at the maximum labeled dose (up to 53.2 mg twice daily for DMD) is not expected to pose a QT prolongation risk.
- 22 March 2026
- Published by Wiley in Clinical Pharmacology in Drug Development
- Vol. 15 (3) , e70047
Open AccessThorough QT Study on the Effect of Therapeutic and Supratherapeutic Dosing of Givinostat in Healthy Volunteers
Givinostat is a class I/II histone deacetylase inhibitor indicated for Duchenne muscular dystrophy (DMD). The study evaluated the effect of therapeutic and supratherapeutic givinostat doses on the QT/QTc interval. Healthy volunteers received each treatment—givinostat hydrochloride monohydrate oral suspension as a therapeutic (100 mg) or supratherapeutic (300 mg) dose, placebo oral suspension, or moxifloxacin oral tablet (positive control, 400 mg)—according to a block randomization scheme. Cardiodynamic assessments were paired with pharmacokinetic samples. A small, clinically non‐relevant effect on mean placebo‐corrected, change‐from‐baseline QTcF (∆∆QTcF) of 5.5 ms was seen after givinostat 100‐mg dose. Clinically relevant QTc prolongation was observed with the supratherapeutic dose, with a mild ∆∆QTcF increase of 13.6 ms. A delay of ≈3 h between T max and the largest effect on the QTc interval was seen for both doses. In the concentration‐QTc analysis, an E max model captured the data better than the prespecified linear model and showed that an effect on ∆∆QTcF exceeding 10 ms could be excluded within the full range of observed givinostat concentrations in this study and up to ≈745 ng/mL. Givinostat at the maximum labeled dose (up to 53.2 mg twice daily for DMD) is not expected to pose a QT prolongation risk.
- Open Access
- 1 March 2024
- Published by Elsevier in Journal of Pharmacological and Toxicological Methods
- Vol. 126, 107498
Virtual clinical QT exposure-response studies – A translational computational approach
- 1 March 2024
- Published by Elsevier in Journal of Pharmacological and Toxicological Methods
- Vol. 126, 107498
Open AccessVirtual clinical QT exposure-response studies – A translational computational approach
- Open Access
- 5 October 2023
- Published by Elsevier in Endocrine Practice
- Vol. 30 (1) , 11-18
Relacorilant, a Selective Glucocorticoid Receptor Modulator in Development for the Treatment of Patients With Cushing Syndrome, Does Not Cause Prolongation of the Cardiac QT Interval
- 5 October 2023
- Published by Elsevier in Endocrine Practice
- Vol. 30 (1) , 11-18
Open AccessRelacorilant, a Selective Glucocorticoid Receptor Modulator in Development for the Treatment of Patients With Cushing Syndrome, Does Not Cause Prolongation of the Cardiac QT Interval