MEROPENEM TRIHYDRATE
MEROPENEM TRIHYDRATE is an intervention with 4 clinical trials. Currently 1 active trials ongoing.
Registry-listed formulations
This catalogue entry has no confirmed scientific concept.
Each study is counted once in the molecule profile. Registry products remain separate. Naming an ingredient does not establish that products are interchangeable or what participants received.
5 source entries across 4 studies. This list may not include all unresolved or historical entries.
- Meropenem Fresenius KabiRegistry product
Linked study entry; product equivalence not established
Formulation reported by source: SOLUTION FOR INJECTION/INFUSION
View study and source - Meropenem Fresenius KabiRegistry product
Linked study entry; product equivalence not established
Formulation reported by source: SOLUTION FOR INJECTION/INFUSION
View study and source - MEROPENEM TRIHYDRATERegistry product
Linked study entry; product equivalence not established
Formulation reported by source: POWDER FOR SOLUTION FOR INJECTION/INFUSION
View study and source - Meropenem AptaPharma 1 g injektio-/infuusiokuiva-aine, liuosta vartenRegistry product
Linked study entry; product equivalence not established
Formulation reported by source: SOLUTION FOR INJECTION/INFUSION
View study and source - Meropenem Fresenius Kabi 1 g pulver till injektionsvätska eller infusionsvätska, lösningRegistry product
Linked study entry; product equivalence not established
Formulation reported by source: SOLUTION FOR INJECTION/INFUSION
View study and source
Success Metrics
Phase Distribution
Phase Distribution
0
Early Stage
0
Mid Stage
2
Late Stage
Highest Phase Reached
Phase 4Trial Status & Enrollment
0.0%
0 of 0 finished
0.0%
0 ended early
1
trials recruiting
4
all time
Detailed Status
Development Timeline
Analytics
Development Status
Trials by Phase
Trials by Status
Recent Activity
Seven Versus Fourteen Days of Treatment in Uncomplicated Staphylococcus Aureus Bacteremia
BETARGET : Randomized trial of individualizing BETA-lactam taRGET combining therapeutic drug monitoring, minimal inhibitory concentration and model-based dose adjustment, in Intensive Care Units patients with gram negative bacilli infection
LIBRETTO: Stimulan™ Local Antibiotic Delivery System Versus 4-Week Systemic Antibiotic Therapy for Diabetic Foot Osteomyelitis – A Prospective, Randomized, Controlled Trial
Accelerated treatment of infectious endocarditis
Clinical Trials (4)
Seven Versus Fourteen Days of Treatment in Uncomplicated Staphylococcus Aureus Bacteremia
BETARGET : Randomized trial of individualizing BETA-lactam taRGET combining therapeutic drug monitoring, minimal inhibitory concentration and model-based dose adjustment, in Intensive Care Units patients with gram negative bacilli infection
LIBRETTO: Stimulan™ Local Antibiotic Delivery System Versus 4-Week Systemic Antibiotic Therapy for Diabetic Foot Osteomyelitis – A Prospective, Randomized, Controlled Trial
Accelerated treatment of infectious endocarditis
All 4 trials loaded
Drug Details
- Intervention Type
- Type not reported
- Total Trials
- 4