Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| Dong-A ST Co., Ltd. | INDUSTRY |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
To evaluate the effectiveness of DA-9801 at 300mg, 600mg, 900mg and placebo, in reducing pain in subjects with diabetic neuropathic pain compared to their baseline values.
This is a double-blind, randomized, parallel group, dose ranging, placebo-controlled study where eligible subjects (age 18 to 75 years) will have an average pain score ≥ 4 on an 11-point Likert numerical rating scale (NRS) for at least four days each week prior to randomization as assessed by daily pain diaries. Eligible subjects will be randomized to a 1:1:1:1 ratio to receive 300mg, 600mg, 900mg of DA-9801, or placebo three times a day for 12 weeks. During and at the end of the 12-week treatment period subjects will be evaluated for safety and efficacy parameters. A follow-up visit for safety will occur two weeks after the last treatment visit (TV).
The Screening Phase (2 weeks) is designed to determine whether subjects are eligible to proceed to the Treatment Phase of the study and consists of a series of screening assessments designed to determine eligibility. Eligible subjects will undergo a two-week washout period for medications and therapies administered for pain management.
At or up to 21 days before the Screening Visit, written informed consent from (ICF) the subject will be obtained by the Investigator or a suitably qualified designee before the performance of any protocol specific procedure. At the Screening Visit, the subject will be issued a daily diary in order to record daily pain level during the screening phase.
The Treatment Phase (TV0 to TV12) begins with a series of assessments designed to confirm the subjects' continued eligibility. The site will collect the daily diary and the subject's pain score will be determined. Only subjects whose average pain score is ≥ 4 for at least four days each week will be randomized to any of the four treatment groups.
DA-9801 administration schedule is three times per day, starting from TV0 to TV12.
During this study phase subjects will be evaluated on a weekly basis. Efficacy evaluations each week will include the subject's global impression of improvement and CGI of pain. Safety evaluations during the Treatment Phase will consist of adverse event assessments at each visit.
The Follow-up Visit (two weeks after last TV) The Follow-up Visit is designed to assess safety and will occur 14 days after the last TV. If the subject is withdrawn from the study prior to TV12, the subject should be exited from the study AFTER completing the specified assessments for that visit.
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| DA-9801 300mg | Experimental | DA-9801 will be administered in tablet form, 100mg taken 3 times daily to subjects randomized to this arm of the study. Subjects will be expected to take this medication for 12 weeks. |
|
| DA-9801 600mg | Experimental | DA-9801 will be administered in tablet form, 200 mg taken 3 times daily to subjects randomized to this arm of the study. Subjects will be expected to take this medication for 12 weeks. |
|
| DA-9801 900mg | Experimental | DA-9801 will be administered in tablet form, 300 mg taken 3 times daily to subjects randomized to this arm of the study. Subjects will be expected to take this medication for 12 weeks. |
|
| Placebo | Placebo Comparator | Placebo (same formulation as DA-9801 but without the active ingredients) will be administered in tablet form, 3 times daily to subjects randomized to this arm of the study. Subjects will be expected to take this tablet for 12 weeks. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| DA-9801 300mg | Drug | 300 mg of DA-9801 in tablet form, 100 mg to be taken 3 times daily for 12 weeks. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change in Clinic Visit Pain Score at the 12 Week Visit Compared to Baseline as Assessed by the 11-point Likert Numerical Rating Scale (NRS) | Pain score was assessed by the subject using the 11-point Likert rating scale for pain (0=no pain to 10=worst possible pain) prior to conduct of any other study assessment. The change in clinic visit pain score at the 12-week visit was compared to baseline. | Baseline to 12 weeks of treatment |
| Measure | Description | Time Frame |
|---|---|---|
| Percentage Change in Clinic Visit Pain Score at the 12-week Visit Compared to Baseline as Assessed by the 11-point Likert Numerical Rating Scale (NRS) | Pain intensity was assessed by the subject before any other protocol procedures at baseline and at the 12- week visit using an 11-point Likert-type numerical rating scale for pain (0=no pain, to 10=worst possible pain) (Negative values indicate percentage reductions). |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Evidence of another type of neuropathic pain caused by a condition other than diabetes
Pain from another source as severe or greater than the pain under study
BMI (Body Mass Index) > 37 kg/m2
Clinical signs of infection related to sores of any type on the legs
Subjects on any investigational drug(s) or therapeutic device(s) within 30 days preceding screening; or subject or physician anticipates use of any of these therapies by the subject during the course of the study
Previous participation in the Treatment Phase of this Protocol
History of drug or alcohol abuse, within the past 6 months
Malignant disease not in remission for 5 years or more that has been medically or surgically treated without evidence of metastases
Presence of one or more medical conditions, as determined by medical history, which seriously compromises the subject's ability to complete the study, including history of poor adherence with medical treatment, renal, hepatic, hematologic, active auto-immune or immune diseases that, in the opinion of the Investigator, would make the subject an inappropriate candidate for this study: c) One or more abnormal blood biochemistry analyte result that is ≥ 3 times that of the upper limit of the normal range; d) For laboratory results that are significantly lower than the normal range, specific criteria will be used to judge subject eligibility for randomization for Total protein, Albumin, and Hemoglobin or Platelets.
Known history of having Acquired Immunodeficiency Syndrome (AIDS) or with a history known to be infected with Human Immunodeficiency Virus (HIV)
New York Heart Association (NYHA) Class III and IV congestive heart failure (CHF), as defined by the following criteria: a)Class III: Symptoms with moderate exertion b)Class IV: Symptoms at rest
Pregnant or breast feeding
Women of child-bearing potential not using an effective birth control method. Women of child-bearing potential are defined as women physiologically capable of becoming pregnant, UNLESS they meet the following criteria:
d) Post-menopausal: 12 months of natural (spontaneous) amenorrhea or 6 months of spontaneous amenorrhea with serum Follicle Stimulating Hormone (FSH) levels > 40mIU/m, OR; e) 6 weeks post surgical bilateral oophorectomy with or without hysterectomy, OR; f) Are using one or more of the following acceptable methods of contraception: surgical sterilization, hormonal contraception, and double-barrier methods. Reliable contraception should be maintained throughout the study and for 7 days after study discontinuation.
Subjects with a diagnosis of psychiatric disorders such as major depressive disorder, bipolar disorder, obsessive compulsive disorder, generalized anxiety, dysthymia or suicidality/suicide ideation
Administration of local anesthetic shot or systemic steroids within two months of screening
Subjects not willing to undergo a two-week washout period for pharmacologic and non-pharmacologic pain management techniques
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Gabriel Maislos, D.P.M | Houston Foot & Ankle Care | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Center for United Research, Inc. | Lakewood | California | 90712 | United States | ||
| Diablo Clinical Research |
Not provided
A total of 185 subjects were screened in this study from which, 128 subjects were randomized to the treatment groups, and 57 subjects were categorized as screen failure. Thirty-two (32) subjects were randomized to each of the four (4) study treatment groups: 900 mg DA-9801, 600 mg DA9801, 300 mg DA-9801 and placebo.
Not provided
| ID | Title | Description |
|---|---|---|
| FG000 | Placebo | Placebo oral tablets three (3) times per day. |
| FG001 | 300 mg DA-9801 | 100 mg oral tablets three (3) times per day for total daily doses of 300 mg |
| Title | Milestones | Reasons Not Completed | |||||
|---|---|---|---|---|---|---|---|
| Overall Study |
|
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| DA-9801 600mg | Drug | 600 mg of DA-9801 in tablet form, 200 mg to be taken 3 times daily for 12 weeks. |
|
| DA-9801 900mg | Drug | 900 mg of DA-9801 in tablet form, to be taken 300 mg to be taken 3 times daily for 12 weeks. |
|
| Placebo | Drug | Placebo, in tablet form, to be taken 3 times daily for 12 weeks. The placebo is the same formulation as DA-9801 except that it does not contain the active pharmaceutical ingredient. |
|
| Baseline and over 12 week treatment period |
| Number of Participants With at Least 30% Improvement Compared to Baseline as Assessed by the 11- Point Likert Numerical Rating Scale (NRS) at the Week 12 Clinic Visit | Pain intensity was assessed by the subject before any other protocol procedures at baseline and week 12 based on 11-point Likert-type numerical rating scale for pain (0=no pain, to 10=worst possible pain). The number of participants who had achieved ≥ a 30% reduction in pain from the baseline was to be compared between the treatment groups and placebo. | Baseline to 12 week treatment period |
| Difference in Average Weekly Pain Score Between Dose Groups as Assessed by Daily Diary | Average 24-hour pain intensity was assessed daily based on the 11-point Likert-type numerical rating scale for pain (0=no pain, to 10=worst possible pain). Average weekly pain scores are defined as 7* [(Pain Day 1 + Pain Day 2 + …+ Pain Day n)]/n where n is the number of available diary entries for the week. The minimum pain score for a week would be 0 and the maximum would be 70. Difference in the average weekly pain score at Week 12 is the score for each week minus the baseline . | Baseline to 12 week treatment period |
| Difference in Average Weekly Most Severe Pain Score Between Dose Groups as Assessed by Daily Diary | Most severe 24-hour pain intensity was assessed daily based on the 11-point Likert-type numerical rating scale for pain (0=no pain, to 10=worst possible pain). Average weekly most severe pain scores are defined as 7* [(Pain Day 1 + Pain Day 2 + …+ Pain Day n)]/n where n is the number of available diary entries for the week. The minimum possible pain score for a week would be 0 and the maximum possible would be 70. Difference in the average weekly pain score at Week 12 is the score at each week minus baseline . | Baseline to 12 week treatment period |
| Difference in Average Weekly Overnight Pain Score Between Dose Groups as Assessed by Daily Diary | Overnight pain intensity was assessed daily based on the 11-point Likert-type numerical rating scale for pain (0=no pain, to 10=worst possible pain). Average weekly overnight pain scores are defined as 7* [(Pain Day 1 + Pain Day 2 + …+ Pain Day n)]/n where n is the number of available diary entries for the week. The minimum possible pain score for a week would be 0 and the maximum possible would be 70. Difference in the average weekly overnight pain score at Week 12 is the score at each week minus baseline | Baseline to 12 week treatment period |
| Change From Baseline Within Group- Difference in Average Weekly Pain Score Compared to Baseline as Assessed by Daily Diary | Average weekly pain intensity was assessed daily based on the 11-point Likert-type numerical rating scale for pain (0=no pain, to 10=worst possible pain). Average weekly pain scores are defined as 7* [(Pain Day 1 + Pain Day 2 + …+ Pain Day n)]/n where n is the number of available diary entries for the week. The minimum possible pain score for a week would be 0 and the maximum possible would be 70. Difference in the average weekly pain score at Week 12 is the score at each week minus baseline. | Baseline to 12 week treatment period |
| Change From Baseline Within Group-Difference in Average Weekly Overnight Pain Score Compared to Baseline as Assessed by Daily Diary | Overnight pain intensity was assessed daily based on the 11-point Likert-type numerical rating scale for pain (0=no pain, to 10=worst possible pain). Average weekly overnight pain scores are defined as 7* [(Pain Day 1 + Pain Day 2 + …+ Pain Day n)]/n where n is the number of available diary entries for the week. The minimum possible pain score for a week would be 0 and the maximum possible would be 70. Difference in the average weekly overnight pain score at Week 12 is the score at each week minus baseline | Baseline to 12 week treatment period |
| Number of Participants Considered to be Responders on Global Impression of Improvement (PGI-I) at Week 12 | PGI measures the subject's overall improvement in pain. The assessment was to be completed each week during the Treatment Phase. Global impression of improvement was assessed by the subject based on a 7 point scale (1-very much improved, 2-much improved, 3-minimally improved, 4-no change, 5-minimally worse, 6-much worse, 7-very much worse. Responders are defined as subjects with response of "very much improved", "much improved" or "minimally improved" | Week 12 |
| Number of Participants Number of Participants Considered to be Responders in Clinical Global Impression (CGI) at Week 12 | CGI measures global severity of illness at a given point of time and the improvement from baseline. The assessment was to be completed by the Investigator at baseline and each week during the treatment phase. CGI responders were defined as subjects achieving a score of: (1): Very much improved or (2): Much improved or (3): Minimally improved on the clinician-rated CGI global improvement item. | Week 12 |
| Average Weekly Rescue Medication Use | During the Treatment Periods, subjects taking 500 mg acetaminophen or Tylenol® for severe pain recorded the frequency and dosage in the daily diary. The use of 500 mg acetaminophen or Tylenol® was recorded for Morning, Afternoon or Evening time. For each subject, the total weekly rescue medication was calculated, and it was used to assess average weekly rescue medication use. | Week 1 to Week 12 |
| Walnut Creek |
| California |
| 94598-3347 |
| United States |
| Clinical Research Consulting, LLC | Milford | Connecticut | 06460 | United States |
| PAB Clinical Research | Brandon | Florida | 33511 | United States |
| Metabolic Research Institute, Inc. | West Palm Beach | Florida | 33401 | United States |
| Johns Hopkins University | Baltimore | Maryland | 21205 | United States |
| Novex Clinical Research, Inc. | New Bedford | Massachusetts | 02740 | United States |
| Albany Medical Center | Albany | New York | 12208 | United States |
| Coastal Carolina Research Center | Mt. Pleasant | South Carolina | 29464 | United States |
| KRK Research | Dallas | Texas | 75230 | United States |
| North Texas Endocrine Center | Dallas | Texas | 75231 | United States |
| Houston Foot & Ankle Care | Houston | Texas | 77074 | United States |
| Wasatch Clinical Research | Salt Lake City | Utah | 84107 | United States |
| Rainier Clinical Research Center, Inc. | Renton | Washington | 98057 | United States |
| FG002 | 600 mg DA-9801 | 200 mg oral tablets three (3) times per day for total daily doses of 600 mg |
| FG003 | 900 mg DA-9801 | 300 mg oral tablets three (3) times per day for total daily doses of 900 mg |
| COMPLETED |
|
| NOT COMPLETED |
|
|
Not provided
| ID | Title | Description |
|---|---|---|
| BG000 | Placebo | Placebo oral tablets three (3) times per day. |
| BG001 | 300 mg DA-9801 | Oral tablets three (3) times per day for total daily doses of 300 mg |
| BG002 | 600 mg DA-9801 | Oral tablets three (3) times per day for total daily doses of 600 mg |
| BG003 | 900 mg DA-9801 | Oral tablets three (3) times per day for total daily doses of 900 mg |
| BG004 | Total | Total of all reporting groups |
| 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 |
| ||||||||||||||||
| Region of Enrollment | Number | participants |
| ||||||||||||||||
| Body Mass Index (BMI) | Mean | Standard Deviation | kg/m^2 |
| |||||||||||||||
| Height | Mean | Standard Deviation | Inches |
| |||||||||||||||
| Weight | Mean | Standard Deviation | lbs |
|
| 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 | Change in Clinic Visit Pain Score at the 12 Week Visit Compared to Baseline as Assessed by the 11-point Likert Numerical Rating Scale (NRS) | Pain score was assessed by the subject using the 11-point Likert rating scale for pain (0=no pain to 10=worst possible pain) prior to conduct of any other study assessment. The change in clinic visit pain score at the 12-week visit was compared to baseline. | Intent-to-Treat (ITT) population - defined as all subjects who were randomized and had an ICF. The ITT population was the primary population for the analysis of primary and secondary endpoints. | Posted | Mean | Standard Deviation | Scores on a scale | Baseline to 12 weeks of treatment |
|
|
| ||||||||||||||||||||||||||||||||||
| Secondary | Percentage Change in Clinic Visit Pain Score at the 12-week Visit Compared to Baseline as Assessed by the 11-point Likert Numerical Rating Scale (NRS) | Pain intensity was assessed by the subject before any other protocol procedures at baseline and at the 12- week visit using an 11-point Likert-type numerical rating scale for pain (0=no pain, to 10=worst possible pain) (Negative values indicate percentage reductions). | Intent-to-Treat (ITT) population - defined as all subjects who were randomized and had an ICF. The ITT population was the primary population for the analysis of primary and secondary endpoints. | Posted | Mean | Standard Deviation | Percentage change | Baseline and over 12 week treatment period |
| ||||||||||||||||||||||||||||||||||||
| Secondary | Number of Participants With at Least 30% Improvement Compared to Baseline as Assessed by the 11- Point Likert Numerical Rating Scale (NRS) at the Week 12 Clinic Visit | Pain intensity was assessed by the subject before any other protocol procedures at baseline and week 12 based on 11-point Likert-type numerical rating scale for pain (0=no pain, to 10=worst possible pain). The number of participants who had achieved ≥ a 30% reduction in pain from the baseline was to be compared between the treatment groups and placebo. | Intent-to-Treat (ITT) population - defined as all subjects who were randomized and had an ICF. The ITT population was the primary population for the analysis of primary and secondary endpoints. | Posted | Count of Participants | Participants | Baseline to 12 week treatment period |
| |||||||||||||||||||||||||||||||||||||
| Secondary | Difference in Average Weekly Pain Score Between Dose Groups as Assessed by Daily Diary | Average 24-hour pain intensity was assessed daily based on the 11-point Likert-type numerical rating scale for pain (0=no pain, to 10=worst possible pain). Average weekly pain scores are defined as 7* [(Pain Day 1 + Pain Day 2 + …+ Pain Day n)]/n where n is the number of available diary entries for the week. The minimum pain score for a week would be 0 and the maximum would be 70. Difference in the average weekly pain score at Week 12 is the score for each week minus the baseline . | Intent-to-Treat (ITT) population - defined as all subjects who were randomized and had an ICF. The ITT population was the primary population for the analysis of primary and secondary endpoints. | Posted | Mean | Standard Deviation | Average weekly group pain score | Baseline to 12 week treatment period |
| ||||||||||||||||||||||||||||||||||||
| Secondary | Difference in Average Weekly Most Severe Pain Score Between Dose Groups as Assessed by Daily Diary | Most severe 24-hour pain intensity was assessed daily based on the 11-point Likert-type numerical rating scale for pain (0=no pain, to 10=worst possible pain). Average weekly most severe pain scores are defined as 7* [(Pain Day 1 + Pain Day 2 + …+ Pain Day n)]/n where n is the number of available diary entries for the week. The minimum possible pain score for a week would be 0 and the maximum possible would be 70. Difference in the average weekly pain score at Week 12 is the score at each week minus baseline . | Intent-to-Treat (ITT) population - defined as all subjects who were randomized and had an ICF. The ITT population was the primary population for the analysis of primary and secondary endpoints. | Posted | Mean | Standard Deviation | weekly most severe pain score | Baseline to 12 week treatment period |
| ||||||||||||||||||||||||||||||||||||
| Secondary | Difference in Average Weekly Overnight Pain Score Between Dose Groups as Assessed by Daily Diary | Overnight pain intensity was assessed daily based on the 11-point Likert-type numerical rating scale for pain (0=no pain, to 10=worst possible pain). Average weekly overnight pain scores are defined as 7* [(Pain Day 1 + Pain Day 2 + …+ Pain Day n)]/n where n is the number of available diary entries for the week. The minimum possible pain score for a week would be 0 and the maximum possible would be 70. Difference in the average weekly overnight pain score at Week 12 is the score at each week minus baseline | Intent-to-Treat (ITT) population - defined as all subjects who were randomized and had an ICF. The ITT population was the primary population for the analysis of primary and secondary endpoints. | Posted | Mean | Standard Deviation | average weekly overnight pain score | Baseline to 12 week treatment period |
| ||||||||||||||||||||||||||||||||||||
| Secondary | Change From Baseline Within Group- Difference in Average Weekly Pain Score Compared to Baseline as Assessed by Daily Diary | Average weekly pain intensity was assessed daily based on the 11-point Likert-type numerical rating scale for pain (0=no pain, to 10=worst possible pain). Average weekly pain scores are defined as 7* [(Pain Day 1 + Pain Day 2 + …+ Pain Day n)]/n where n is the number of available diary entries for the week. The minimum possible pain score for a week would be 0 and the maximum possible would be 70. Difference in the average weekly pain score at Week 12 is the score at each week minus baseline. | Intent-to-Treat (ITT) population - defined as all subjects who were randomized and had an ICF. The ITT population was the primary population for the analysis of primary and secondary endpoints. | Posted | Mean | Standard Deviation | average weekly pain score | Baseline to 12 week treatment period |
| ||||||||||||||||||||||||||||||||||||
| Secondary | Change From Baseline Within Group-Difference in Average Weekly Overnight Pain Score Compared to Baseline as Assessed by Daily Diary | Overnight pain intensity was assessed daily based on the 11-point Likert-type numerical rating scale for pain (0=no pain, to 10=worst possible pain). Average weekly overnight pain scores are defined as 7* [(Pain Day 1 + Pain Day 2 + …+ Pain Day n)]/n where n is the number of available diary entries for the week. The minimum possible pain score for a week would be 0 and the maximum possible would be 70. Difference in the average weekly overnight pain score at Week 12 is the score at each week minus baseline | Intent-to-Treat (ITT) population - defined as all subjects who were randomized and had an ICF. The ITT population was the primary population for the analysis of primary and secondary endpoints. | Posted | Mean | Standard Deviation | average weekly overnight pain score | Baseline to 12 week treatment period |
| ||||||||||||||||||||||||||||||||||||
| Secondary | Number of Participants Considered to be Responders on Global Impression of Improvement (PGI-I) at Week 12 | PGI measures the subject's overall improvement in pain. The assessment was to be completed each week during the Treatment Phase. Global impression of improvement was assessed by the subject based on a 7 point scale (1-very much improved, 2-much improved, 3-minimally improved, 4-no change, 5-minimally worse, 6-much worse, 7-very much worse. Responders are defined as subjects with response of "very much improved", "much improved" or "minimally improved" | Intent-to-Treat (ITT) population - defined as all subjects who were randomized and had an ICF. The ITT population was the primary population for the analysis of primary and secondary endpoints. | Posted | Count of Participants | Participants | Week 12 |
| |||||||||||||||||||||||||||||||||||||
| Secondary | Number of Participants Number of Participants Considered to be Responders in Clinical Global Impression (CGI) at Week 12 | CGI measures global severity of illness at a given point of time and the improvement from baseline. The assessment was to be completed by the Investigator at baseline and each week during the treatment phase. CGI responders were defined as subjects achieving a score of: (1): Very much improved or (2): Much improved or (3): Minimally improved on the clinician-rated CGI global improvement item. | Intent-to-Treat (ITT) population - defined as all subjects who were randomized and had an ICF. The ITT population was the primary population for the analysis of primary and secondary endpoints. | Posted | Count of Participants | Participants | Week 12 |
| |||||||||||||||||||||||||||||||||||||
| Secondary | Average Weekly Rescue Medication Use | During the Treatment Periods, subjects taking 500 mg acetaminophen or Tylenol® for severe pain recorded the frequency and dosage in the daily diary. The use of 500 mg acetaminophen or Tylenol® was recorded for Morning, Afternoon or Evening time. For each subject, the total weekly rescue medication was calculated, and it was used to assess average weekly rescue medication use. | Intent-to-Treat (ITT) population - defined as all subjects who were randomized and had an ICF. The ITT population was the primary population for the analysis of primary and secondary endpoints. | Posted | Mean | Standard Deviation | mg | Week 1 to Week 12 |
|
Treatment-Emergent Adverse Events (TEAEs) started on or after the first randomized study treatment administration and monitored for 14 weeks through study completion.
Not provided
Not provided
| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Placebo | Placebo oral tablets three (3) times per day. | 3 | 32 | 14 | 32 | ||
| EG001 | 300 mg DA-9801 | 100 mg oral tablets three (3) times per day for total daily doses of 300 mg | 0 | 32 | 21 | 32 | ||
| EG002 | 600 mg DA-9801 | 200 mg oral tablets three (3) times per day for total daily doses of 600 mg | 2 | 32 | 16 | 32 | ||
| EG003 | 900 mg DA-9801 | 300 mg oral tablets three (3) times per day for total daily doses of 900 mg | 0 | 32 | 8 | 32 |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Coronary artery disease | Cardiac disorders | MedDRA 16.1 | Non-systematic Assessment |
| |
| Hyperglycemia | Metabolism and nutrition disorders | MedDRA 16.1 | Non-systematic Assessment |
| |
| Ketoacidosis | Metabolism and nutrition disorders | MedDRA 16.1 | Non-systematic Assessment |
| |
| Mania | Psychiatric disorders | MedDRA 16.1 | Non-systematic Assessment |
| |
| Asthma | Respiratory, thoracic and mediastinal disorders | MedDRA 16.1 | Non-systematic Assessment |
| |
| Peripheral ischaemia | Vascular disorders | MedDRA 16.1 | Non-systematic Assessment |
|
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Constipation | Gastrointestinal disorders | MedDRA 16.1 | Non-systematic Assessment |
| |
| Diarrhea | Gastrointestinal disorders | MedDRA 16.1 | Non-systematic Assessment |
| |
| Nausea | Gastrointestinal disorders | MedDRA 16.1 | Non-systematic Assessment |
| |
| Vomiting | Gastrointestinal disorders | MedDRA 16.1 | Non-systematic Assessment |
| |
| Oedema peripheral | Gastrointestinal disorders | MedDRA 16.1 | Non-systematic Assessment |
| |
| Nasopharyngitis | Infections and infestations | MedDRA 16.1 | Non-systematic Assessment |
| |
| Pneumonia | Infections and infestations | MedDRA 16.1 | Non-systematic Assessment |
| |
| Upper respiratory tract infection | Infections and infestations | MedDRA 16.1 | Non-systematic Assessment |
| |
| Urinary tract infection | Infections and infestations | MedDRA 16.1 | Non-systematic Assessment |
| |
| Arthralgia | Musculoskeletal and connective tissue disorders | MedDRA 16.1 | Non-systematic Assessment |
| |
| Back pain | Musculoskeletal and connective tissue disorders | MedDRA 16.1 | Non-systematic Assessment |
| |
| Pain in extremity | Musculoskeletal and connective tissue disorders | MedDRA 16.1 | Non-systematic Assessment |
| |
| Headache | Nervous system disorders | MedDRA 16.1 | Non-systematic Assessment |
| |
| Cough | Respiratory, thoracic and mediastinal disorders | MedDRA 16.1 | Non-systematic Assessment |
| |
| Oropharyngeal pain | Respiratory, thoracic and mediastinal disorders | MedDRA 16.1 | Non-systematic Assessment |
| |
| Rhinorrhea | Respiratory, thoracic and mediastinal disorders | MedDRA 16.1 | Non-systematic Assessment |
| |
| Pruritus | Skin and subcutaneous tissue disorders | MedDRA 16.1 | Non-systematic Assessment |
| |
| Hypertension | Vascular disorders | MedDRA 16.1 | Non-systematic Assessment |
|
Not provided
Not provided
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Vice President Clinical Operations | NeuroBo Pharmaceuticals, Inc. | 617-313-7331 | nikki.shannon@neurobopharma.com |
| ID | Term |
|---|---|
| D003929 | Diabetic Neuropathies |
| D003920 | Diabetes Mellitus |
| D010146 | Pain |
| ID | Term |
|---|---|
| D010523 | Peripheral Nervous System Diseases |
| D009468 | Neuromuscular Diseases |
| D009422 | Nervous System Diseases |
| D048909 | Diabetes Complications |
| D004700 | Endocrine System Diseases |
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
Not provided
Not provided
| ID | Term |
|---|---|
| C562027 | DA-9801 |
Not provided
Not provided
Not provided
| Male |
|
| Not Hispanic or Latino |
|
| Unknown or Not Reported |
|
| Asian |
|
| Native Hawaiian or Other Pacific Islander |
|
| Black or African American |
|
| White |
|
| More than one race |
|
| Unknown or Not Reported |
|
| TV 12 |
|
Oral tablets three (3) times per day for total daily doses of 900 mg |
|
|
| 900 mg DA-9801 |
Oral tablets three (3) times per day for total daily doses of 900 mg |
|
|
| OG003 | 900 mg DA-9801 | Oral tablets three (3) times per day for total daily doses of 900 mg |
|
|
| OG003 | 900 mg DA-9801 | Oral tablets three (3) times per day for total daily doses of 900 mg |
|
|
| OG003 | 900 mg DA-9801 | Oral tablets three (3) times per day for total daily doses of 900 mg |
|
|
| OG003 | 900 mg DA-9801 | Oral tablets three (3) times per day for total daily doses of 900 mg |
|
|
| OG003 | 900 mg DA-9801 | Oral tablets three (3) times per day for total daily doses of 900 mg |
|
|
| 900 mg DA-9801 |
Oral tablets three (3) times per day for total daily doses of 900 mg |
|
|
Oral tablets three (3) times per day for total daily doses of 900 mg |
|
|
Oral tablets three (3) times per day for total daily doses of 900 mg
|
|