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Trial · Interventional

CompletedPhase 1/2Results postedRegistry data

Clinical Trial to Investigate CT38 in the Treatment of Myalgic Encephalomyelitis / Chronic Fatigue Syndrome

Short name InTiME

This trial does not test a peptide that PepBank tracks.

  • Names ACTH (corticotropin), does not test it. It appears in the conditions.

Overview

Status
Completed
Phase
Phase 1/2
Enrollment
17 participants (actual)
Sponsor
LUCINDA BATEMAN, MD · Other
Design
Not randomized · Open label (no masking)
Countries
1 country

United States

Start
23 Jul 2018
Primary completion
30 Apr 2019
Completion
30 Apr 2019
First posted
2 Aug 2018
Last update posted
12 May 2020
Conditions
Myalgic Encephalomyelitis · Chronic Fatigue Syndrome

Timeline

1 trial · 1 completed · 1 with posted results

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
201820192020
  1. Ph 1/2

    InTiME

    NCT03613129

    23 Jul 2018 to 30 Apr 2019

Registry summary

Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.

This study seeks to investigate the safety, tolerability and efficacy of CT38, an experimental peptide administered by subcutaneous infusion, in the treatment of ME/CFS patients.

Interventions

  • CT38Drug

Arms4

  • Active comparator

    D0.20

    Subcutaneous infusion of CT38 at 0.20 μg/kg/hour, for 3 hours on each of 2 days

  • Active comparator

    D0.03

    Subcutaneous infusion of CT38 at 0.03 μg/kg/hour, for 3.5 hours on each of 3 days

  • Active comparator

    D0.06

    Subcutaneous infusion of CT38 at 0.06 μg/kg/hour, for 3.5 hours on each of 3 days

  • Active comparator

    D0.01

    Subcutaneous infusion of CT38 at 0.01 μg/kg/hour, for 3.5 hours on each of 3 days

Primary outcomes1

Outcomes the sponsor listed as primary.

  1. Total Daily Symptom Score (TDSS)

    Time frame · 28 days preceding Visit 3 (pre-treatment) and 28 days preceding Visit 6 (post-treatment)

    Registry description

    Pre-/post-treatment difference in TDSS (0-65 scale, 0=no symptoms; 65=maximum of 5 for each of 13 specific patient-reported symptoms). The TDSS sums the patient-reported daily symptom score for each of 13 specific symptoms (including fatigue, muscle/joint pain, sleep problems, cognitive problems, orthostatic intolerance, body temperature perceptions, flu-like symptoms, headaches or sensitivities, shortness of breath, gastrointestinal problems, urogenital problems, anxiety and depression), each assessed on a 0-5 scale (0=no symptom, 1=very mild, 2=mild, 3=moderate, 4=severe, 5=severe)

Secondary outcomes(2)
  1. SF-36, PCS

    Time frame · Visit 3 before treatment (pre-treatment) and at Visit 6 (post-treatment)

    Registry description

    Pre-/post-treatment difference in the physical component score (PCS) of the RAND 36-Item Health Survey (SF-36), on a 0-100 scale (where 0=max disability and 100=no disability)

  2. SF-36, MCS

    Time frame · Visit 3 before treatment (pre-treatment) and at Visit 6 (post-treatment)

    Registry description

    Pre-/post-treatment difference in the mental component score (MCS) of the RAND 36-Item Health Survey (SF-36), on a 0-100 scale (where 0=max disability and 100=no disability)

Posted results

Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.

Primary outcome results

Primary outcomeMean· 28 days preceding Visit 3 (pre-treatment) and 28 days preceding Visit 6 (post-treatment)

Total Daily Symptom Score (TDSS)

GroupValue (units on a scale)Spread
Intent-to-treat29.59.4
D0.0128.712.2
D0.0329.211.4
D0.0631.31.3
D0.2030.18.0
Secondary and other outcome results(2)
Secondary outcomeMean· Visit 3 before treatment (pre-treatment) and at Visit 6 (post-treatment)

SF-36, PCS

GroupValue (units on a scale)Spread
Intent-to-treat27.94.0
D0.0125.96.9
D0.0324.63.7
D0.0627.61.4
D0.2030.61.4
Secondary outcomeMean· Visit 3 before treatment (pre-treatment) and at Visit 6 (post-treatment)

SF-36, MCS

GroupValue (units on a scale)Spread
Intent-to-treat34.03.6
D0.0136.33.2
D0.0328.93.9
D0.0632.13.2
D0.2035.82.6

Adverse events, as posted

Adverse events as posted: participants affected out of participants at risk, by group
GroupDeathsSerious eventsOther events
Intent-to-treatAll patients receiving test drug0 / 141 / 1414 / 14
D0.01Subcutaneous infusion of CT38 at 0.01 μg/kg/hour, for 3.5 hours on each of 3 days0 / 30 / 33 / 3
D0.03Subcutaneous infusion of CT38 at 0.03 μg/kg/hour, for 3.5 hours on each of 3 days0 / 70 / 77 / 7
D0.06Subcutaneous infusion of CT38 at 0.06 μg/kg/hour, for 3.5 hours on each of 3 days0 / 20 / 22 / 2
D0.20Subcutaneous infusion of CT38 at 0.20 μg/kg/hour, for 3 hours on each of 2 days0 / 21 / 22 / 2

Each cell reads participants affected / participants at risk, as the registry posted them.

Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works

Studies0

Studies that cite this trial.

No study cites this trial.

Other registry references

References listed at the registry that are not in PepBank. They link to PubMed.

  • DerivedPereira G, Gillies H, Chanda S, Corbett M, Vernon SD, Milani T, Bateman L. Acute Corticotropin-Releasing Factor Receptor Type 2 Agonism Results in Sustained Symptom Improvement in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. Front Syst Neurosci. 2021 Sep 1;15:698240. doi: 10.3389/fnsys.2021.698240. eCollection 2021. PMID 34539356

Eligibility

Who could join, as posted.

Sex
All
Age
from 18 Years up to 60 Years
Healthy volunteers
Not accepted
Inclusion and exclusion criteria, as posted
Inclusion Criteria: * Provision of signed and dated informed consent form * Ability to read, understand and speak English * Living at an altitude between 3,500 and 5,500 feet above sea level for the past 1 year * Willing to perform an exercise test * Diagnosed with ME/CFS and meet the following 3 case definitions: Fukuda Research Case Definition for CFS (1994), Revised Canadian Consensus Criteria for ME/CFS (2010) and the Institute of Medicine (IOM) Clinical Diagnostic Criteria for ME/CFS (2015) * Relatively stable state of illness for the individual patient over the past 3 months * Male or female, between the ages of 18 and 60 years old * Males or females of reproductive potential agree to remain abstinent or use (or have their partner use) 2 acceptable methods of contraception, starting from the time of informed consent through 28 days after the last dose of study drug. Acceptable methods of birth control during the study are intrauterine device, diaphragm with spermicide, contraceptive sponge, condom or vasectomy. Oral contraceptive pills may not be used as the sole method of contraception because the effect of CT38 on the efficacy of oral contraceptive pills has not yet been established * Stated willingness to comply with all study procedures and remain available for the study duration * Have mobile (smart) phone and access to the internet Exclusion Criteria: * Alternate medical or psychiatric illness that could explain the ME/CFS symptoms * Unwilling or unable to perform an exercise test * Active or uncontrolled co-morbidities which in the opinion of the PI may interfere with the ability of the patient to participate in the study. Co-morbidities may include acute infection, Crohn's disease, diabetes mellitus (Type 1 or Type 2, evidenced by a history of glycated hemoglobin (A1C) \> 7 at any time), Guillain-Barre syndrome, lupus, multiple sclerosis, myasthenia gravis, rheumatoid arthritis, or other such diseases that may be exclusionary. Particularly conditions or medications that cause immunodeficiency or immunosuppression will be excluded. Examples of such conditions can be found in the tables "Causes of Secondary Immunodeficiency" and "Some Drugs that Cause Immunosuppression" in the "Merck Manual" * Pregnancy, or while breast feeding. Women should not be enrolled within 6 months of giving birth and within 3 months of cessation of breast feeding * A Body Mass Index \> 35 * Cigarette smoker or former smoker who has smoked within 6 months of the start of the study * Living at an altitude that is more than 1,000 feet (lower or higher) from the study site (which is 4,500 feet above sea level) * History of: * Major depression with psychotic or melancholic features before the diagnosis of ME/CFS, or active depression (major depression with psychotic or melancholic features) as determined by self-report * Untreated endocrine diagnoses including hypothyroidism (Hashimoto's, etc.), Grave's disease, adrenal insufficiency, hypogonadism (testosterone deficiency), diabetes mellitus or insipidus * Acute infection within the past 30 days * Within the last 3 years, any significant head injury, e.g., concussion with loss of consciousness, brain surgery, an automobile accident with head/neck injury, other traumatic brain injury * A supra-ventricular tachycardia or ventricular tachycardia, e.g., atrial fibrillation or flutter, paroxysmal atrial fibrillation, junctional tachycardia, ventricular tachycardia * Severe baseline hypotension defined as rested sitting systolic BP \< 100 mmHg or rested sitting diastolic BP \< 60 mmHg * Renal impairment based upon the local lab normal estimated glomerular filtration rate (eGFR) (drug is cleared by passive renal filtration) * Known hypersensitivity or clinically significant allergies to tromethamine or Tween 80 (both excipients in the drug product) * Substance abuse in the past 12 months as determined by self-report * Improvement in overall ME/CFS symptoms as a result of any treatment intervention in the past 3 months * Current treatment with medications that interact with pathways involving: (i) 5-hydroxytryptamine (5HT) (e.g., selective 5HT re-uptake inhibitors or selective serotonin reuptake inhibitors (SSRIs), 5HT and norepinephrine re-uptake inhibitors or serotonin and norepinephrine reuptake inhibitors (SNRIs), tricyclic antidepressants, monoamine oxidase inhibitors, triptans); (ii) norepinephrine (e.g., adrenergic agonists or antagonists, norepinephrine re-uptake inhibitors, norepinephrine and dopamine re- uptake inhibitors); (iii) dopamine (e.g., norepinephrine and dopamine re-uptake inhibitors); and (iv) cortisol pathways (e.g., oral glucocorticoids, fludrocortisone). * Prior treatment with * Short-term (\< 2 weeks) antiviral or antibiotic medication or flu shot within the past 4 weeks * Long-term (\> 2 weeks) antiretrovirals within the past 12 months * RituximabTM within 6 months * Any new prescription drug or herbal remedy within 2 weeks prior to the onset of the trial * Current participation in another clinical treatment trial

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