Clinical trial · Interventional
Intramuscular Injections of Degarelix Administered in 1-Month Dosing Regimens in Patients With Prostate Cancer
Open-label, Multi-centre, Parallel Group Dose-Escalation Trial Assessing the Pharmacokinetics, Pharmacodynamics, Efficacy and Safety of Intramuscular Injections of Degarelix Administered in 1-Month Dosing Regimens in Patients With Prostate Cancer
NCT01491971CI-TRIAL-00012973IM1completedPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Intramuscular Injections of Degarelix Administered in 1-Month Dosing Regimens in Patients with Prostate Cancer.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Prostate Cancer | Malignant Prostate Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Degarelix | Drug | Degarelix | ALIAS |
Design
Arms and outcomes
Arms (3)
- type
- EXPERIMENTAL
- label
- Degarelix - Cohort 1
- description
- (gonadotrophin-releasing hormone (GnRH) receptor blocker)
- interventionNames
- Drug: Degarelix
- type
- EXPERIMENTAL
- label
- Degarelix - Cohort 2
- description
- (gonadotrophin-releasing hormone (GnRH) receptor blocker)
- interventionNames
- Drug: Degarelix
- type
- EXPERIMENTAL
- label
- Degarelix - Cohort 3
- description
- (gonadotrophin-releasing hormone (GnRH) receptor blocker)
Eligibility
Eligibility (as posted)
- Sex
- Male
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Has a histologically confirmed adenocarcinoma of the prostate, for which endocrine therapy is indicated * Has a current tumour, nodule and metastasis (TNM) staging within 12 weeks prior to treatment start and, if clinically indicated a bone scan * Has a PSA level meeting one of these criteria: 1. For treatment-naïve patients: Screening PSA level should be ≥2 ng/mL. 2. For patients with recurrence after radical prostatectomy: Patients should have a serum PSA increase of ≥0.2 ng/mL from the previous test on two consecutive measurements 3. For patients with recurrence after radiotherapy or cryotherapy: Patients should have a serum PSA (two measurements) to be \>2 ng/mL higher than a previously confirmed PSA nadir * Has a screening serum testosterone level above the lower limit of normal range in an elderly male population, globally defined as \>150 ng/dL * Has an Eastern Cooperative Oncology Group score of ≤2 * Has a life expectancy of at least one year Exclusion Criteria: * Has had previous or is currently under hormonal management of prostate cancer * Is considered to be a candidate for curative therapy i.e. radical prostatectomy or radiotherapy during the trial period * Has a history of bilateral orchiectomy, adrenalectomy, or hypophysectomy * Has a marked baseline prolongation of QT/QTcF interval (e.g. repeated demonstration of a QTcF interval \>450 ms) * Has a history of risk factors for Torsade de Pointes ventricular arrhythmias (e.g. heart failure, hypokalemia, or family history of Long QT Syndrome) * Has a previous history or presence of another malignancy, other than prostate * Currently receiving chronic treatment with intramuscular medication injected into the ventrogluteal or dorsogluteal muscle * Has received an investigational drug within the last 28 days preceding the Screening Visit or longer if considered to possibly influence the outcome of the current trial
References
Publications (0)
Data not yet available
No reference posted for this study.