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ShareScore release 0.9.0
Dataset results
17 results for “oral testosterone undecanoate”
Ambulatory Blood Pressure Monitoring in Oral Testosterone Undecanoate (TU, LPCN 1021) Treated Hypogonadal Men
ClinicalTrials.gov study NCT03868059. IPD Sharing: NO. Countries: 1. Publications: 1.
Open-label, Follow-up Study of Oral Testosterone Undecanoate in Hypogonadal Men
ClinicalTrials.gov study NCT01699178. IPD Sharing: NO. Countries: 2. Publications: 1.
Safety and Efficacy Trial of Oral Testosterone Undecanoate (TU) in Hypogonadal Men
ClinicalTrials.gov study NCT01403116. IPD Sharing: NO. Countries: 2. Publications: 1.
Efficacy and Safety of Oral Testosterone Undecanoate in Hypogonadal Men
ClinicalTrials.gov study NCT03198728. IPD Sharing: NO. Countries: 1. Publications: 1.
Ambulatory Blood Pressure Monitoring (ABPM) Extension Study of Oral Testosterone Undecanoate in Hypogonadal Men
ClinicalTrials.gov study NCT04467697. IPD Sharing: NO. Countries: 1. Publications: 1.
Concordance table for oral testosterone undecanoate
<p>Concordance analysis was performed to identify the best post-dose T assay time-point to guide any necessary dose-adjustment in oral TU patients. Concordance is defined herein to describe the extent of agreement between a decision to adjust the oral TU dose (up or down) when a single circulating T concentration in remains in the hypogonadal range [i.e., <252 ng/dl (9 nmol/L) for this study] or supraphysiological range [i.e., >907 ng/dL (31 nmol/L)] and the desired outcome of that decision (i.e., a circulating T level in the eugonadal range) is achieved.</p>
An Open-Label Study of 50 Mg Oral Testosterone Undecanoate (Kyztrex) in Menopausal Women with Low Testosterone and HSDD
ClinicalTrials.gov study NCT06082817. IPD Sharing: NO. Countries: 1. Publications: 6.
Dosing Validation Study of Oral Testosterone Undecanoate (TU, LPCN 1021).
ClinicalTrials.gov study NCT03242590. IPD Sharing: NO. Countries: 0. Publications: 1.
Concordance table for oral testosterone undecanoate
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Supplementary Appendix: Efficacy and safety analysis of a new oral testosterone undecanoate (TU) formulation following two years of treatment in hypogonadal men
<p>Supplementary Table 1. Change from Baseline in Efficacy and Safety Parameters over Two<br> Years of Oral TU Treatment – Confirmatory Analysis</p> <p>Supplementary Figure 1. Study Dose Titration Scheme for Days 0-180</p> <p>Supplementary Figure 2. Study Dose Titration Scheme for Days 180 and 270</p> <p>Supplementary Figure 3. Study Dose Titration Scheme for Days 365 Through End of Study</p>
Single-Dose Pharmacokinetics of Oral Testosterone Undecanoate With and Without Concomitant Inhibition of UGT2B17
ClinicalTrials.gov study NCT06312761. IPD Sharing: Not stated. Countries: 0. Publications: 16.
A Study of Oral Testosterone Undecanoate (TU) in Hypogonadal Men
ClinicalTrials.gov study NCT02722278. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
The Effect of Various Amounts of Fat on PK of Oral Testosterone Undecanoate
ClinicalTrials.gov study NCT02921386. IPD Sharing: NO. Countries: 1. Publications: 0.
Study to Determine the Effect of Food on the Absorption of an Oral Testosterone Undecanoate Formulation
ClinicalTrials.gov study NCT00924612. IPD Sharing: Not stated. Countries: 2. Publications: 0.
Patient Satisfaction After Switching to Oral Testosterone Undecanoate
ClinicalTrials.gov study NCT04983940. IPD Sharing: NO. Countries: 1. Publications: 0.
Safety and Efficacy of Oral Testosterone Undecanoate Followed by Enzalutamide as Therapy for Men With Metastatic Castrate Resistant Prostate Cancer
ClinicalTrials.gov study NCT05081193. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Dosing Flexibility Study of Oral Testosterone Undecanoate (TU, LPCN 1021)
ClinicalTrials.gov study NCT03242408. IPD Sharing: NO. Countries: 0. Publications: 0.
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