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Business decision to stop the program
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Multicenter, open-label, long-term extended access treatment protocol in adult patients with a primary diagnosis of MDD.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Rapastinel | Experimental | Rapastinel 450 mg (prefilled syringe, weekly or biweekly or up to 4 weeks at the investigator's discretion intravenous IV administration) |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Rapastinel | Drug | Rapastinel 450 mg (prefilled syringe, weekly or biweekly or up to 4 weeks at the investigator's discretion intravenous IV administration) |
|
| Measure | Description | Time Frame |
|---|---|---|
| Count of Participants Experiencing One or More Treatment Emergent Adverse Events (TEAEs) | A Treatment Emergent Adverse Event was considered any unfavorable and unintended sign, symptom, or disease associated with the use of the study drug, whether or not considered related to the study drug. An Adverse Drug Reaction was a harmful and unintended reaction that is incurred during routine administration or use of the drug, whose causal relationship with the drug cannot be excluded. | Up to 45 Weeks |
Not provided
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Inclusion Criteria:
Exclusion Criteria:
Suicide risk, as determined by meeting any of the following criteria:
At imminent risk of injuring self or others or causing significant damage to property, as judged by the investigator
Females who are pregnant, breastfeeding, or planning to become pregnant or breastfeed during participation
Females of childbearing potential and male partners of females of childbearing potential, not using a reliable means of contraception
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| Name | Affiliation | Role |
|---|---|---|
| Jenna Hoogerheyde | Allergan | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Alabama at Birmingham | Birmingham | Alabama | 35294 | United States | ||
| Harmonex Neuroscience Research |
Not provided
| Label | URL |
|---|---|
| Additional information on study locations near you may be found at AllerganClinicalTrials.com. For any study not on AllerganClinicalTrials.com, please contact IR-CTRegistration@Allergan.com for assistance. | View source |
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Patients from RAP-MD-99, completed 1 of the rapastinel lead-in studies - RAP-MD-04, RAP-MD-05, RAP-MD-06 or RAP-MD-33.
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| ID | Title | Description |
|---|---|---|
| FG000 | Rapastinel | Rapastinel 450 mg (prefilled syringe, weekly or biweekly or up to 4 weeks at the investigator's discretion intravenous IV administration) |
| Title | Milestones | Reasons Not Completed | |||||
|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot | Yes | No | No | Study Protocol | Jul 3, 2018 | Jul 1, 2020 |
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| Dothan |
| Alabama |
| 36303 |
| United States |
| NoesisPharma | Phoenix | Arizona | 85016 | United States |
| Woodland International Research Group | Little Rock | Arkansas | 72211 | United States |
| Woodland Research Northwest | Rogers | Arkansas | 72758 | United States |
| California Pharmaceutical Research Institute, Inc | Anaheim | California | 92804 | United States |
| Southern California Research LLC. | Beverly Hills | California | 90036 | United States |
| ATP Clinical Research Inc. | Costa Mesa | California | 92626 | United States |
| ProScience Research Group | Culver City | California | 90230 | United States |
| Pharmacology Research Institute | Encino | California | 91316 | United States |
| Behavioral Research Specialists, LLC | Glendale | California | 91206 | United States |
| Sun Valley Research Center | Imperial | California | 92251 | United States |
| Irvine Center for Clinical Research, Inc | Irvine | California | 92614 | United States |
| Synergy Clinical Research Center of Escondido | Lemon Grove | California | 91945 | United States |
| Pharmacology Research Institute | Los Alamitos | California | 90720 | United States |
| CITrials | Riverside | California | 92506 | United States |
| California Neuroscience Research | Sherman Oaks | California | 91403 | United States |
| Viking Clinical Research | Temecula | California | 92591 | United States |
| Pacific Clinical Research Medical | Upland | California | 91786 | United States |
| Comprehensive Psychiatric Care | Norwich | Connecticut | 06360 | United States |
| Gulfcoast Clinical Research Center | Fort Myers | Florida | 33912 | United States |
| Reliable Clinical Research | Hialeah | Florida | 33012 | United States |
| Meridien Research | Lakeland | Florida | 33805 | United States |
| Innovative Clinical Research, Inc | Lauderhill | Florida | 33319 | United States |
| Research Centers of America | Oakland Park | Florida | 33334 | United States |
| Medical Research Group of Central Florida | Orange City | Florida | 32763 | United States |
| David A. Medina, MD | Orlando | Florida | 32819 | United States |
| Institute for Advanced Medical Research | Atlanta | Georgia | 30341 | United States |
| iResearch Atlanta, LLC | Decatur | Georgia | 30030 | United States |
| Northwest Behavioral Research Center | Marietta | Georgia | 30060 | United States |
| Attalla Consultants, LLC | Smyrna | Georgia | 30082 | United States |
| Alexian Brothers Center for Psychiatric Research | Hoffman Estates | Illinois | 60169 | United States |
| Capstone Clinical Research | Libertyville | Illinois | 60048 | United States |
| AMR - Baber Research, Inc. | Naperville | Illinois | 60563 | United States |
| University of Kansas School of Medicine Clinical Trial Unit | Wichita | Kansas | 67214 | United States |
| Lake Charles Clinical Trials | Lake Charles | Louisiana | 70629 | United States |
| Louisiana Clinical Research | Shreveport | Louisiana | 71101 | United States |
| ActivMed Practices & Research, Inc. | Methuen | Massachusetts | 01844 | United States |
| Coastal Research Associates | South Weymouth | Massachusetts | 02190 | United States |
| University of Massachusetts Medical School | Worcester | Massachusetts | 01655 | United States |
| Precise Research Centers | Flowood | Mississippi | 39232 | United States |
| Psychiatric Care and Research Center | O'Fallon | Missouri | 63368 | United States |
| St. Charles Psychiatric Associates | Saint Charles | Missouri | 63304 | United States |
| Premier Psychiatric Research Institute, LLC | Lincoln | Nebraska | 68526 | United States |
| Healthy Perspectives - Innovative Mental Health Services. PLLC | Nashua | New Hampshire | 03060 | United States |
| Bio Behavioral Health | Toms River | New Jersey | 08755 | United States |
| Albuquerque Neuroscience, Inc | Albuquerque | New Mexico | 87109 | United States |
| SPRI Clinical Trials, LLC | Brooklyn | New York | 11235 | United States |
| Manhattan Behavioral Medicine | New York | New York | 10022 | United States |
| Finger Lakes Clinical Research | Rochester | New York | 14618 | United States |
| Richmond Behavioral Associates | Staten Island | New York | 10312 | United States |
| Patient Priority Clinical Sites | Cincinnati | Ohio | 45215 | United States |
| The Ohio State University Department of Psychiatry | Columbus | Ohio | 43210 | United States |
| Midwest Clinical Research Center LLC | Dayton | Ohio | 45417 | United States |
| Professional Psychiatric Services | Mason | Ohio | 45040 | United States |
| Red River Medical Research Center, LLC | Oklahoma City | Oklahoma | 73112 | United States |
| Sooner Clinical Research, Inc | Oklahoma City | Oklahoma | 73112 | United States |
| Paradigm Research Professionals | Oklahoma City | Oklahoma | 73118 | United States |
| Summit Research Network LLC | Portland | Oregon | 97210 | United States |
| Lehigh Center for Clinical Research | Allentown | Pennsylvania | 18104 | United States |
| Dr. Cherian Verghese | Norristown | Pennsylvania | 19403 | United States |
| Carolina Clinical Trials, Inc. | Charleston | South Carolina | 29407 | United States |
| Coastal Carolina Research Center | Mt. Pleasant | South Carolina | 29464 | United States |
| Research Strategies of Memphis, LLC | Memphis | Tennessee | 38119 | United States |
| Donald J. Garcia, Jr., MD, PA | Austin | Texas | 78737 | United States |
| Community Clinical Research | Austin | Texas | 78754 | United States |
| Houston Clinical Trials | Bellaire | Texas | 77401 | United States |
| North Texas Clinical Trials | Fort Worth | Texas | 76104 | United States |
| Earle Research | Houston | Texas | 77058 | United States |
| Red Oak Psychiatry Associates, PA | Houston | Texas | 77090 | United States |
| Clinical Trials of Texas | San Antonio | Texas | 78229 | United States |
| Grayline Clinical Drug Trials | Wichita Falls | Texas | 76309 | United States |
| Psychiatric and Behavioral Solutions | Salt Lake City | Utah | 84105 | United States |
| Psychiatric Alliance of the Blue Ridge, Inc | Charlottesville | Virginia | 22903 | United States |
| COMPLETED |
|
| NOT COMPLETED |
|
|
The Open-label Safety Population will consist of all participants who signed the RAP-MD-99 ICF and who received at least 1 dose of open-label rapastinel during the OLTP of the protocol.
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| ID | Title | Description |
|---|---|---|
| BG000 | Rapastinel | Rapastinel 450 mg (prefilled syringe, weekly or biweekly or up to 4 weeks at the investigator's discretion intravenous IV administration) |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean | Standard Deviation | Years |
| |||||||||||||||||
| Sex: Female, Male | Count of Participants | Participants |
| ||||||||||||||||||
| Ethnicity (NIH/OMB) | Count of Participants | Participants |
| ||||||||||||||||||
| Race (NIH/OMB) | Count of Participants | Participants |
| ||||||||||||||||||
| Weight | Mean | Standard Deviation | kg |
| |||||||||||||||||
| Height | Median | Standard Deviation | cm |
| |||||||||||||||||
| BMI | Mean | Standard Deviation | kg/m^2 |
|
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Count of Participants Experiencing One or More Treatment Emergent Adverse Events (TEAEs) | A Treatment Emergent Adverse Event was considered any unfavorable and unintended sign, symptom, or disease associated with the use of the study drug, whether or not considered related to the study drug. An Adverse Drug Reaction was a harmful and unintended reaction that is incurred during routine administration or use of the drug, whose causal relationship with the drug cannot be excluded. | The Open-label Safety Population will consist of all participants who signed the RAP-MD-99 ICF and who received at least 1 dose of open-label rapastinel during the OLTP of the protocol. | Posted | Number | Participants | Up to 45 Weeks |
|
|
|
Up to 45 Weeks
The Open-label Safety Population will consist of all participants who signed the RAP-MD-99 ICF and who received at least 1 dose of open-label rapastinel during the OLTP of the protocol.
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Rapastinel | Rapastinel 450 mg (prefilled syringe, weekly or biweekly or up to 4 weeks at the investigator's discretion intravenous IV administration) | 0 | 230 | 4 | 230 | 14 | 230 |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Ventricular tachycardia | Cardiac disorders | MedDRA Version 22.0 | Systematic Assessment |
| |
| Device malfunction | Product Issues | MedDRA Version 22.0 | Systematic Assessment |
| |
| Pericardial effusion | Cardiac disorders | MedDRA Version 22.0 | Systematic Assessment |
| |
| Pneumonia | Infections and infestations | MedDRA Version 22.0 | Systematic Assessment |
| |
| Abortion spontaneous | Pregnancy, puerperium and perinatal conditions | MedDRA Version 22.0 | Systematic Assessment |
| |
| Rib fracture | Injury, poisoning and procedural complications | MedDRA Version 22.0 | Systematic Assessment |
| |
| Skin laceration | Injury, poisoning and procedural complications | MedDRA Version 22.0 | Systematic Assessment |
| |
| Road traffic accident | Injury, poisoning and procedural complications | MedDRA Version 22.0 | Systematic Assessment |
|
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Dysgeusia | Nervous system disorders | MedDRA Version 22.0 | Systematic Assessment |
|
A disclosure restriction on the PI is that the sponsor can review results communications prior to public release and can embargo communications regarding trial results for a period that is less than or equal to 90 days from the time submitted to the sponsor for review. The sponsor cannot require changes to the communication and cannot extend the embargo.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Therapeutic Area, Head | Allergan | 714-246-4500 | IR-CTRegistration@allergan.com |
| Prot_000.pdf |
| SAP | No | Yes | No | Statistical Analysis Plan | Aug 21, 2019 | Jul 1, 2020 | SAP_001.pdf |
| ID | Term |
|---|---|
| D003865 | Depressive Disorder, Major |
| D003863 | Depression |
| ID | Term |
|---|---|
| D003866 | Depressive Disorder |
| D019964 | Mood Disorders |
| D001523 | Mental Disorders |
| D001526 | Behavioral Symptoms |
| D001519 | Behavior |
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| ID | Term |
|---|---|
| C507283 | GLYX-13 peptide |
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| Unknown or Not Reported |
|
| Native Hawaiian or Other Pacific Islander |
|
| Black or African American |
|
| White |
|
| More than one race |
|
| Unknown or Not Reported |
|