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Pilot Study of Minocycline (NPL-2003) in Adults With Obsessive-Compulsive Disorder (OCD)

Pilot Study of Minocycline (NPL-2003) in Adults With Obsessive-Compulsive Disorder (OCD)

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00728923
Enrollment
9
Registered
2008-08-06
Start date
2008-08-31
Completion date
2011-07-31
Last updated
2012-04-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obsessive Compulsive Disorder

Keywords

OCD

Brief summary

Obsessive-compulsive disorder (OCD) is a common psychiatric illness that affects up to 2-3% of the population. People with OCD experience anxiety-provoking, intrusive thoughts, known as obsessions, and feel compelled to perform repetitive behaviors, or compulsions. The only medications proven effective for OCD are serotonin reuptake inhibitors (SRIs), but even with SRI treatment, most patients continue to experience significant OCD symptoms, impaired functioning, and diminished quality of life. Recent evidence suggest that a different neurotransmitter, glutamate, may contribute to the symptoms in OCD. Medications that target glutamate hold promise for ameliorating symptoms for those patients continuing to suffer from OCD. In this study we are recruiting patients to receive the drug NPL-2003, which is thought to modulate the neurotransmitter glutamate, added to whatever other OCD medications they are taking in a 12-week open label study.

Interventions

DRUGNPL-2003

Minocycline (NPL-2003) daily for 12 weeks

Sponsors

New York State Psychiatric Institute
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Primary DSM-IV Diagnosis of OCD * Currently on a stable and adequate dose of SRI (or history of prior SRI or CBT treatment meeting criteria for adequate trial) * Patients not currently receiving an SRI or CBT will be included if they have undergone a prior SRI or CBT trial and they report no interest in pursuing another DRI or CBT trial at this time. Patients who have been on SRIs in the past must be free of SRIs for at least 6 weeks prior to participation * Y-BOCS score of greater or equal to 16 * Physically health and females must be using effective contraception * Sufficient severity of symptoms to warrant additional augmentation treatment * Able to provide consent

Exclusion criteria

* Ongoing treatment with other antibiotics and/or Accutane. Patients with lupus erythematosus * Patients planning to start CBT during the study period or those who have begun CBT within the past 8 weeks * Presence of psychotic symptoms or lifetime history of schizophrenia, bipolar disorder or other psychotic disorder * Current major depressive disorder (patients must be free of the disorder for 3 months prior to enrollment). HAM-D must be \<18. * Judged clinically to be at risk of suicide (suicidal ideation, severe depression or other factors * Current eating disorder * Severe renal insufficiency * Documented history of hypersensitivity or intolerance to tetracycline antibiotics * Concomitant use of anti-coagulant drugs, antacids, iron, calcium, magnesium, aluminum, zinc sales. Note:Concomitant psychotropic medications such as antipsychotics and benzodiazepines will be permitted as long as they have been stable for at least 4 weeks and remain stable during the course of the study. * Current ETOH/drug abuse or dependence disorder of dependency in the past 3 months * Female patients who are either pregnant or nursing

Design outcomes

Primary

MeasureTime frameDescription
Number of Patients Who Met and Exceeded Response Criteria of Yale-Brown Obsessive-Compulsive Scale12 weeksPatients given YBOCS (Yale Brown Obsessive-Compulsive Scale), a gold standard measure of obsessions and compulsions. For the YBOCS the minimum units are 0 and Maximum units on the total scale are 40. The higher the number on the YBOCS, the more severe the symptoms. Response was defined as at least a 30% reduction on the YBOCS.

Secondary

MeasureTime frameDescription
Number of Patients That Met Response Criteria for the Hamilton Depression Rating Scale.12 weeksPatients given HAM-D (Hamilton Depression Scale), a measure of depressive symptoms. For the HAM-D the minimum units are 0 and Maximum units on the total scale are 50. The higher the number on the HAM-D, the more severe the symptoms. Response was defined as at least a 30% reduction on the HAM-D.

Countries

United States

Participant flow

Recruitment details

Adult outpatients were recruited from the community starting August 2008 until July 2011.

Participants by arm

ArmCount
Minocycline
minocycline 100mg bid for 12 weeks
9
Total9

Baseline characteristics

CharacteristicMinocycline
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
0 Participants
Age, Categorical
Between 18 and 65 years
9 Participants
Age Continuous37 years
STANDARD_DEVIATION 15
Region of Enrollment
United States
9 participants
Sex: Female, Male
Female
3 Participants
Sex: Female, Male
Male
6 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
— / —
other
Total, other adverse events
0 / 9
serious
Total, serious adverse events
0 / 9

Outcome results

Primary

Number of Patients Who Met and Exceeded Response Criteria of Yale-Brown Obsessive-Compulsive Scale

Patients given YBOCS (Yale Brown Obsessive-Compulsive Scale), a gold standard measure of obsessions and compulsions. For the YBOCS the minimum units are 0 and Maximum units on the total scale are 40. The higher the number on the YBOCS, the more severe the symptoms. Response was defined as at least a 30% reduction on the YBOCS.

Time frame: 12 weeks

ArmMeasureValue (NUMBER)
MinocyclineNumber of Patients Who Met and Exceeded Response Criteria of Yale-Brown Obsessive-Compulsive Scale2 participants
Secondary

Number of Patients That Met Response Criteria for the Hamilton Depression Rating Scale.

Patients given HAM-D (Hamilton Depression Scale), a measure of depressive symptoms. For the HAM-D the minimum units are 0 and Maximum units on the total scale are 50. The higher the number on the HAM-D, the more severe the symptoms. Response was defined as at least a 30% reduction on the HAM-D.

Time frame: 12 weeks

ArmMeasureValue (NUMBER)
MinocyclineNumber of Patients That Met Response Criteria for the Hamilton Depression Rating Scale.0 participants

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026