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Moxidectin

Phase 1

Healthy | Small molecule | Other |Pfizer, Inc.|Last Updated: Feb 15, 2011

Success Probability

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Market & Valuation

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Trial Design

UNCONTROLLED
Total Trials1
Total Enrollment38

FDA Designations

No designations recorded

Clinical trial landscape

Moxidectin · 3 trials · 2 indications

Phase 1 3
NCT00856362Study Evaluating The Co-Administration Of Moxidectin And Midazolam In Healthy SubjectsHealthy
COMPLETED38 Analytics
NCT00736697Study Evaluating The Effect Of High-Fat Meal On Bioavailability And Pharmacokinetics Of Single Dose Of MoxidectinInfection
COMPLETED54 Analytics
NCT00751764Study Evaluating The Excretion Of Moxidectin Into The Breast Milk Of Lactating, Non-Breastfeeding WomenInfection
COMPLETED12 Analytics
PHASE1COMPLETED
Study Evaluating The Co-Administration Of Moxidectin And Midazolam In Healthy Subjects
HealthyUnlock trial analytics
PHASE1COMPLETED
Study Evaluating The Effect Of High-Fat Meal On Bioavailability And Pharmacokinetics Of Single Dose Of Moxidectin
InfectionUnlock trial analytics
PHASE1COMPLETED
Study Evaluating The Excretion Of Moxidectin Into The Breast Milk Of Lactating, Non-Breastfeeding Women
InfectionUnlock trial analytics

Study Endpoints

Primary Endpoints

Blood samples will be collected for determination of moxidectin and midazolam plasma concentrations
4 months
Blood samples
4 months

Secondary Endpoints

Safety based on adverse event monitoring, physical examinations, vital sign measurements, 12-lead electrocardiograms (ECGs) and routine lab tests
4 months
Electrocardiograms
4 months
Safety based on adverse event monitoring, vital sign measurements, 12-lead ECGs and routine lab tests.
4 months
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Study Design & Arms

AllocationNON_RANDOMIZED
MaskingNONE
ModelSINGLE_GROUP
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
1EXPERIMENTAL -

Interventions

NameTypeDescription
MoxidectinDRUG -
MidazolamDRUG -
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Eligibility Criteria

Age Range18 Years to 50 Years
SexALL
Healthy VolunteersYes
Study Sites1

Inclusion criteria: 1. Men or women of nonchildbearing potential (WONCBP) aged 18 to 50 years inclusive at screening. WONCBP may be included if they are either surgically sterile (hysterectomy and/or oophorectomy) or postmenopausal for ≥1 year (with follicle-stimulating hormone \[FSH\] ≥38 mIU/...

Countries:GermanyFranceUnited Kingdom
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Frequently asked questions about Moxidectin

What is Moxidectin used for?

Moxidectin is an investigational small molecule being studied in healthy volunteers and for infection. It is in Phase 1 clinical development. The drug has been evaluated in trials for its pharmacokinetics, excretion into breast milk, and potential drug interactions, though it is not approved for any indication.

Who makes Moxidectin?

Moxidectin is being developed by Pfizer, Inc., which trades under the ticker symbol PFE. The company is conducting early-stage clinical research on this small molecule drug candidate.

What phase is Moxidectin in?

Moxidectin is in Phase 1 clinical development. It is an investigational drug, meaning it has not been approved by regulatory authorities. All completed trials for Moxidectin are Phase 1 studies, and no active trials are currently listed.

What clinical trials is Moxidectin in?

Moxidectin has completed three Phase 1 trials. NCT00736697 studied the effect of a high-fat meal on bioavailability in 54 participants in France. NCT00751764 examined excretion into breast milk in 12 lactating women in the UK. NCT00856362 evaluated co-administration with midazolam in 38 healthy subjects in Germany.

Is Moxidectin the same as other drugs?

Moxidectin is a distinct small molecule drug candidate. No alternative names have been reported for this compound. It is being studied independently by Pfizer for potential use in infections and healthy volunteer studies.