A Phase 1 interventional study of ELX-02 and Placebo in Genetic Disease and Nonsense Mutation, sponsored by Eloxx Pharmaceuticals, Inc.. Completed at 1 site in Belgium. Open to participants aged 18 Years to 55 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-03-16.
Sponsored by Eloxx Pharmaceuticals, Inc. · Phase 1, Interventional, and Treatment
Phase 1 Multiple Ascending Dose Study in Normal Healthy Volunteers
This is a study in humans of ELX-02, an advanced synthetic aminoglycoside optimized as a translational read-through drug (TRID) for the treatment of genetic conditions caused by nonsense mutations. This is a classical Phase 1b study designed as a randomized, double-blinded, placebo-controlled, multiple dose escalation to evaluate the safety, tolerability, and pharmacokinetics of ELX-02 in healthy adult volunteers.
583 studies on the registry are indexed under Genetic Diseases, Inborn; 157 are open to participants now.
This study's enrollment of 62 is above the median of 40 across 305 interventional studies indexed under Genetic Diseases, Inborn.
Browse Genetic Diseases, Inborn studies →Eloxx Pharmaceuticals, Inc. is the lead sponsor of 9 studies on the registry; 1 is open to participants now.
Counted across the registry records on this site, refreshed daily.
Inclusion criteria: Subjects must meet all of the following inclusion criteria to be eligible for enrollment into the study:
Healthy female subjects and male subjects who, at the time of screening, are between the ages of 18 and 55 years, inclusive.
Healthy is defined as no abnormalities identified by a detailed medical history, full physical examination, including blood pressure (BP) and pulse rate measurement, 12-lead (ECG), and clinical laboratory tests.
Female subjects of non- must meet at least one of the following criteria:
Exclusion criteria: Subjects with any of the following characteristics/conditions will not be included in the study:
Subjects with any abnormality at screening, that indicates the presence of a vestibular pathology, conductive hearing loss or balance problem (by an ENT).
Subjects with abnormalities in audiometry results at screening as follows: any pure-tone threshold >55 dB and/or inter-ear difference in any frequency of >20 dB.
Dizziness Handicap Inventory (DHI)-H score>16. Tinnitus Handicap Inventory (THI)-H score >14.
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.
A recording of the heart’s electrical activity, taken with stickers on the chest, arms and legs. It takes a few minutes and does not hurt.
Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).
Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.
Periods have stopped for good: usually no period for 12 months in a row without another medical reason, sometimes confirmed by a blood test (FSH).
Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.
Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.
GFR (glomerular filtration rate) is how much blood the kidneys filter each minute. It is usually estimated from a blood test — eGFR, by formulas such as CKD-EPI or MDRD — and some studies ask for it to be measured directly instead. Usually given in mL/min/1.73 m².
Check the method, the units and the minimum the study states. A value of 90 or above is in the normal-or-high range, but kidney damage can show in other tests too.
How quickly the kidneys clear creatinine, a waste product, from the blood. A study may estimate it from a blood test with age, weight and sex (often by the Cockcroft–Gault formula), or measure it using blood and urine collected over a set time. Given in mL/min; higher is better.
The human immunodeficiency virus, which weakens the immune system.
Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.
Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.
Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.
Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.
After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.
Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.
What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.
A drug or device being studied in a clinical trial.
It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.
On an ECG, the QT interval is the time the heart’s lower chambers take to activate electrically and recover in each beat. QTc is that time adjusted for heart rate (QTcF by Fridericia’s formula, QTcB by Bazett’s). Some medicines lengthen it, and a long QTc can raise the risk of a dangerous heart rhythm.
The study may name a correction formula and a limit in milliseconds, often around 450–480.
Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.
Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.
A yellow substance made when red blood cells are broken down, which the liver clears. A high level can mean a problem with the liver or the bile ducts.
Criteria often allow more for people with Gilbert’s syndrome, a harmless inherited condition that raises bilirubin.
The top of the normal range for a blood test, as set by the laboratory that runs it. Each lab prints its own range next to your result.
“≤ 2.5 × ULN” means the result can be up to two and a half times that top value.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Clinically significant
Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
ECG (electrocardiogram)
A recording of the heart’s electrical activity, taken with stickers on the chest, arms and legs. It takes a few minutes and does not hurt.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Childbearing potential
Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).
Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Postmenopausal
Periods have stopped for good: usually no period for 12 months in a row without another medical reason, sometimes confirmed by a blood test (FSH).
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Contraception
Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.
Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
GFR and eGFR (kidney filtering)
GFR (glomerular filtration rate) is how much blood the kidneys filter each minute. It is usually estimated from a blood test — eGFR, by formulas such as CKD-EPI or MDRD — and some studies ask for it to be measured directly instead. Usually given in mL/min/1.73 m².
Check the method, the units and the minimum the study states. A value of 90 or above is in the normal-or-high range, but kidney damage can show in other tests too.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Creatinine clearance (CrCl)
How quickly the kidneys clear creatinine, a waste product, from the blood. A study may estimate it from a blood test with age, weight and sex (often by the Cockcroft–Gault formula), or measure it using blood and urine collected over a set time. Given in mL/min; higher is better.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
HIV
The human immunodeficiency virus, which weakens the immune system.
Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Hepatitis B tests
Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.
Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Hepatitis C tests
Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.
After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
BMI (body mass index)
Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.
What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Investigational drug or device
A drug or device being studied in a clinical trial.
It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
QT and QTc
On an ECG, the QT interval is the time the heart’s lower chambers take to activate electrically and recover in each beat. QTc is that time adjusted for heart rate (QTcF by Fridericia’s formula, QTcB by Bazett’s). Some medicines lengthen it, and a long QTc can raise the risk of a dangerous heart rhythm.
The study may name a correction formula and a limit in milliseconds, often around 450–480.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
ALT and AST (liver enzymes)
Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.
Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Bilirubin
A yellow substance made when red blood cells are broken down, which the liver clears. A high level can mean a problem with the liver or the bile ducts.
Criteria often allow more for people with Gilbert’s syndrome, a harmless inherited condition that raises bilirubin.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
ULN (upper limit of normal)
The top of the normal range for a blood test, as set by the laboratory that runs it. Each lab prints its own range next to your result.
“≤ 2.5 × ULN” means the result can be up to two and a half times that top value.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Placebo
Drug: Placebo
ELX-02
Drug: ELX-02
ELX-02 is a synthetic, designer eukaryotic ribosomal specific glycoside (ERSG) optimized as a translational read-through drug
Placebo
Pharmacokinetic Parameters - Plasma AUC0-24
Day 1 Area under the curve (AUC0-24) of ELX-02 plasma concentration following the subcutaneous (SC) dose on Day 1 to 24 hours post-ose
Time frame: Day 1: pre-dose, 15 min, 30 min, 45 min, 1h, 3h, 6h, 12h, 24h, post-dose
Pharmacokinetic Parameters- Plasma AUC0-24
Day 29 Area under the curve (AUC0-24) of ELX-02 plasma concentration following the subcutaneous (SC) dose on Day 29 to 24 hours post-dose
Time frame: Day 29: pre-dose, 15 min, 30 min, 45 min, 1h, 3h, 6h, 12h, 24h, post-dose
Pharmacokinetic Parameters - Plasma Cmax
Day 1 Peak Plasma Concentration (Cmax) of ELX-02 following the subcutaneous (SC) dose on Day 1 to 72 hours post-dose
Time frame: Day 1: pre-dose, 15 min, 30 min, 45 min, 1h, 3h, 6h, 12h, 24h, 36h, 48h, 72h, post-dose
Pharmacokinetic Parameters - Plasma Cmax
Day 29 Peak Plasma Concentration (Cmax) of ELX-02 following the subcutaneous (SC) dose on Day 29 to 72 hours post-dose
Time frame: Day 29: pre-dose, 15 min, 30 min, 45 min, 1h, 3h, 6h, 12h, 24h, 36h, 48h, 72h post-dose
Pharmacokinetic Parameter - Plasma AUC0-inf
Day 1 Area under the curve (AUC0-inf) of ELX-02 plasma concentration following the subcutaneous (SC) dose on Day 1 extrapolated to infinity
Time frame: Day 1: pre-dose, 15 min, 30 min, 45 min, 1h, 3h, 6h, 12h, 24h, 36h, 48h, 72h post dose
Pharmacokinetic Parameter - Plasma AUC0-inf
Day 29 Area under the curve (AUC0-inf) of ELX-02 plasma concentration following the subcutaneous (SC) dose on Day 29 extrapolated to infinity
Time frame: Day 29: pre-dose, 15 min, 30 min, 45 min, 1h, 3h, 6h, 12h, 24h, 36h, 48h, 72h post dose
Pharmacokinetic Parameter - Plasma Tmax
Day 1 Time to maximum concentration (Tmax) of ELX-02 plasma concentrations following the subcutaneous (SC) dose on Day 1
Time frame: Day 1: pre-dose, 15 min, 30 min, 45 min, 1h, 3h, 6h, 12h, 24h, 36h, 48h, 72h post-dose
Pharmacokinetic Parameter Plasma - Tmax
Day 29 Time to maximum concentration (Tmax) of ELX-02 plasma concentrations following the subcutaneous (SC) dose on Day 29
Time frame: Day 29: pre-dose, 15 min, 30 min, 45 min, 1h, 3h, 6h, 12h, 24h, 36h, 48h, 72h post-dose
Pharmacokinetic Parameter - Plasma Rac(AUC24h)
Accumulation ratio, calculated as AUC24h Day29/AUC24h Day 1
Time frame: Day 1 and Day 24 hr
Pharmacokinetic Parameter - Plasma RAC(Cmax)
Accumulation ratio, calculated as Cmax Day29/Cmax Day 1
Time frame: Day 1 and Day 29
Urine Pharmacokinetics Parameter - Ae72h
Day 1 Cumulative amount of unchanged drug excreted into urine (Ae72h) of ELX-02 following the subcutaneous (SC) dose on Day 1
Time frame: Day 1: pre-dose and during 0-12h, 12-24h, 24-48h, and 48-72h post-dose
Urine Pharmacokinetics Parameter - Ae72h
Day 29 Cumulative amount of unchanged drug excreted into urine (Ae72h) of ELX-02 following the subcutaneous (SC) dose on Day 29
Time frame: Day 29: pre-dose and during 0-12h, 12-24h, 24-48h, and 48-72h post-dose
Urine Pharmacokinetic Parameter - Rmax
Day 1 Maximum rate of urinary extraction (Rmax) of EXL-02 in each collection time interval following the subcutaneous (SC) dose on Day 1
Time frame: Day 1: pre-dose and during 0-12h, 12-24h, 24-48h, and 48-72h post-dose
Urine Pharmacokinetic Parameter - Rmax
Day 29 Maximum rate of urinary extraction (Rmax) of ELX-02 in each collection time interval following the subcutaneous (SC) dose on Day 29
Time frame: Day 29: pre-dose and during 0-12h, 12-24h, 24-48h, and 48-72h post-dose
Urine Pharmacokinetics Parameter - Fe12h Day 1
Percent of dose excreted (Fe) in urine on Day 1
Time frame: 12 hours
Urine Pharmacokinetics Parameter - Fe 12h on Day 29
Percent of dose excreted (Fe) in urine on Day 29
Time frame: 12 h on Day 29
Urine Pharmacokinetics Parameter - CLR24h on Day 1
Renal clearance on Day 1 (CLR=Ae24h/plasmaAUC24h)
Time frame: 24 hours
Urine Pharmacokinetics Parameter - CLR24h
Renal clearance on Day 29 (CLR=Ae24h/plasmaAUC24h)
Time frame: 24 h
Number of Patients Experiencing at Least One Treatment-Emergent Adverse Events (TEAEs)
TEAEs are undesirable events not present prior to medical treatment, or an already present event that worsens either in intensity or frequency following the study treatment
Time frame: Day 1-29
All subjects were treated at medical clinics. The first patient was enrolled on 22 November 2017 and the last subject visit occurred on 18 July 2019.
| Milestone | Cohort 1 | Cohort 2 | Cohort 3 | Cohort 4 | Cohort 5 | Cohort 6 | Cohort 7 | All Placebo |
|---|---|---|---|---|---|---|---|---|
| Started | 6 | 5 | 6 | 6 | 6 | 6 | 6 | 21 |
| Completed | 6 | 5 | 6 | 5 | 5 | 6 | 3 | 19 |
| Not completed | 0 | 0 | 0 | 1 | 1 | 0 | 3 | 2 |
| Withdrew: Adverse event | 0 | 0 | 0 | 1 | 0 | 0 | 2 | 1 |
| Withdrew: Withdrawal by subject | 0 | 0 | 0 | 0 | 1 | 0 | 1 | 1 |
Day 1 Area under the curve (AUC0-24) of ELX-02 plasma concentration following the subcutaneous (SC) dose on Day 1 to 24 hours post-ose
| ng*h/mL | Cohort 1 | Cohort 2 | Cohort 3 and Cohort 5 | Cohort 4 and Cohort 6 | Cohort 7 |
|---|---|---|---|---|---|
| Pharmacokinetic Parameters - Plasma AUC0-24 | 1105.126 ± 15.261 | 3125.484 ± 13.836 | 11018.22 ± 12.436 | 28235.823 ± 16.255 | 61906.528 ± 20.455 |
Day 29 Area under the curve (AUC0-24) of ELX-02 plasma concentration following the subcutaneous (SC) dose on Day 29 to 24 hours post-dose
| ng*h/mL | Cohort 1 | Cohort 2 | Cohort 3 and Cohort 5 | Cohort 4 and Cohort 6 | Cohort 7 |
|---|---|---|---|---|---|
| Pharmacokinetic Parameters- Plasma AUC0-24 | 1215.098 ± 15.431 | 3109.978 ± 16.601 | 10847.306 ± 14.098 | 29651.700 ± 23.223 | 54749.370 ± 13.770 |
Day 1 Peak Plasma Concentration (Cmax) of ELX-02 following the subcutaneous (SC) dose on Day 1 to 72 hours post-dose
| ng/mL | Cohort 1 | Cohort 2 | Cohort 3 and Cohort 5 | Cohort 4 and Cohort 6 | Cohort 7 |
|---|---|---|---|---|---|
| Pharmacokinetic Parameters - Plasma Cmax | 284.710 ± 21.060 | 1003.266 ± 5.766 | 2880.233 ± 11.647 | 7721.256 ± 6.387 | 15912.090 ± 17.265 |
Day 29 Peak Plasma Concentration (Cmax) of ELX-02 following the subcutaneous (SC) dose on Day 29 to 72 hours post-dose
| ng/mL | Cohort 1 | Cohort 2 | Cohort 3 and Cohort 5 | Cohort 4 and Cohort 6 | Cohort 7 |
|---|---|---|---|---|---|
| Pharmacokinetic Parameters - Plasma Cmax | 342.779 ± 12.021 | 961.448 ± 7.460 | 2806.966 ± 16.403 | 7852.172 ± 12.342 | 15435.789 ± 13.872 |
Day 1 Area under the curve (AUC0-inf) of ELX-02 plasma concentration following the subcutaneous (SC) dose on Day 1 extrapolated to infinity
| ng*hr/mL | Cohort 1 | Cohort 2 | Cohort 3 and Cohort 5 | Cohort 4 and Cohort 6 | Cohort 7 |
|---|---|---|---|---|---|
| Pharmacokinetic Parameter - Plasma AUC0-inf | 1107.272 ± 15.345 | 3127.964 ± 13.898 | 11036.305 ± 12.631 | 28335.680 ± 16.468 | 62142.763 ± 20.712 |
Day 29 Area under the curve (AUC0-inf) of ELX-02 plasma concentration following the subcutaneous (SC) dose on Day 29 extrapolated to infinity
| ng*h/mL | Cohort 1 | Cohort 2 | Cohort 3 and Cohort 5 | Cohort 4 and Cohort 6 | Cohort 7 |
|---|---|---|---|---|---|
| Pharmacokinetic Parameter - Plasma AUC0-inf | 1216.448 ± 15.428 | 3114.486 ± 16.704 | 10862.927 ± 14.239 | 29778.143 ± 23.469 | 54933.538 ± 13.979 |
Day 1 Time to maximum concentration (Tmax) of ELX-02 plasma concentrations following the subcutaneous (SC) dose on Day 1
| hour | Cohort 1 | Cohort 2 | Cohort 3 and Cohort 5 | Cohort 4 and Cohort 6 | Cohort 7 |
|---|---|---|---|---|---|
| Pharmacokinetic Parameter - Plasma Tmax | 1.00 (0.50 to 3.00) | 0.75 (0.50 to 1.00) | 1.00 (0.75 to 1.00) | 1.00 (0.75 to 1.00) | 0.86 (0.73 to 1.00) |
Day 29 Time to maximum concentration (Tmax) of ELX-02 plasma concentrations following the subcutaneous (SC) dose on Day 29
| hour | Cohort 1 | Cohort 2 | Cohort 3 and Cohort 5 | Cohort 4 and Cohort 6 | Cohort 7 |
|---|---|---|---|---|---|
| Pharmacokinetic Parameter Plasma - Tmax | 1.00 (0.50 to 1.00) | 0.75 (0.75 to 1.00) | 1.00 (0.75 to 1.00) | 0.75 (0.75 to 1.00) | 0.98 (0.73 to 0.98) |
Accumulation ratio, calculated as AUC24h Day29/AUC24h Day 1
| Ratio | Cohort 1 | Cohort 2 | Cohort 3 and Cohort 5 | Cohort 4 and Cohort 6 | Cohort 7 |
|---|---|---|---|---|---|
| Pharmacokinetic Parameter - Plasma Rac(AUC24h) | 1.093 ± 7.497 | 0.995 ± 6.622 | 0.984 ± 7.892 | 1.056 ± 14.161 | 0.911 ± 13.377 |
Accumulation ratio, calculated as Cmax Day29/Cmax Day 1
| Ratio | Cohort 1 | Cohort 2 | Cohort 3 and Cohort 5 | Cohort 4 and Cohort 6 | Cohort 7 |
|---|---|---|---|---|---|
| Pharmacokinetic Parameter - Plasma RAC(Cmax) | 1.217 ± 15.278 | 0.958 ± 7.429 | 0.976 ± 12.401 | 1.018 ± 15.413 | 0.941 ± 1.262 |
Day 1 Cumulative amount of unchanged drug excreted into urine (Ae72h) of ELX-02 following the subcutaneous (SC) dose on Day 1
| mg | Cohort 1 | Cohort 2 | Cohort 3 and Cohort 5 | Cohort 4 and Cohort 6 | Cohort 7 |
|---|---|---|---|---|---|
| Urine Pharmacokinetics Parameter - Ae72h | 6.702 ± 16.721 | 15.177 ± 8.524 | 58.270 ± 20.046 | 160.665 ± 11.622 | 332.467 ± 18.102 |
Day 29 Cumulative amount of unchanged drug excreted into urine (Ae72h) of ELX-02 following the subcutaneous (SC) dose on Day 29
| mg | Cohort 1 | Cohort 2 | Cohort 3 and Cohort 5 | Cohort 4 and Cohort 6 | Cohort 7 |
|---|---|---|---|---|---|
| Urine Pharmacokinetics Parameter - Ae72h | 6.331 ± 28.505 | 15.021 ± 9.189 | 66.354 ± 15.505 | 162.609 ± 12.742 | 399.302 ± 14.863 |
Day 1 Maximum rate of urinary extraction (Rmax) of EXL-02 in each collection time interval following the subcutaneous (SC) dose on Day 1
| mg/h | Cohort 1 | Cohort 2 | Cohort 3 and Cohort 5 | Cohort 4 and Cohort 6 | Cohort 7 |
|---|---|---|---|---|---|
| Urine Pharmacokinetic Parameter - Rmax | 1.846 ± 30.561 | 4.759 ± 6.706 | 16.132 ± 15.540 | 41.587 ± 21.200 | 69.304 ± 13.495 |
Day 29 Maximum rate of urinary extraction (Rmax) of ELX-02 in each collection time interval following the subcutaneous (SC) dose on Day 29
| mg/h | Cohort 1 | Cohort 2 | Cohort 3 and Cohort 5 | Cohort 4 and Cohort 6 | Cohort 7 |
|---|---|---|---|---|---|
| Urine Pharmacokinetic Parameter - Rmax | 1.950 ± 37.938 | 5.028 ± 15.875 | 18.327 ± 23.862 | 40.607 ± 18.389 | 89.796 ± 14.725 |
Percent of dose excreted (Fe) in urine on Day 1
| percentage of drug excreted | Cohort 1 | Cohort 2 | Cohort 3 and Cohort 5 | Cohort 4 and Cohort 6 | Cohort 7 |
|---|---|---|---|---|---|
| Urine Pharmacokinetics Parameter - Fe12h Day 1 | 79.572 ± 10.030 | 79.440 ± 6.178 | 76.028 ± 17.403 | 89.639 ± 9.227 | 83.362 ± 5.495 |
Percent of dose excreted (Fe) in urine on Day 29
| percentage of drug excreted | Cohort 1 | Cohort 2 | Cohort 3 and Cohort 5 | Cohort 4 and Cohort 6 | Cohort 7 |
|---|---|---|---|---|---|
| Urine Pharmacokinetics Parameter - Fe 12h on Day 29 | 76.095 ± 14.874 | 78.398 ± 3.615 | 88.130 ± 15.218 | 88.914 ± 4.157 | 94.219 ± 7.407 |
Renal clearance on Day 1 (CLR=Ae24h/plasmaAUC24h)
| L/h | Cohort 1 | Cohort 2 | Cohort 3 and Cohort 5 | Cohort 4 and Cohort 6 | Cohort 7 |
|---|---|---|---|---|---|
| Urine Pharmacokinetics Parameter - CLR24h on Day 1 | 5.871 ± 22.645 | 4.823 ± 9.834 | 5.251 ± 19.135 | 5.653 ± 22.959 | 5.331 ± 16.660 |
Renal clearance on Day 29 (CLR=Ae24h/plasmaAUC24h)
| L/h | Cohort 1 | Cohort 2 | Cohort 3 and Cohort 5 | Cohort 4 and Cohort 6 | Cohort 7 |
|---|---|---|---|---|---|
| Urine Pharmacokinetics Parameter - CLR24h | 5.152 ± 29.234 | 4.784 ± 10.828 | 6.068 ± 17.200 | 5.435 ± 28.521 | 7.239 ± 7.903 |
TEAEs are undesirable events not present prior to medical treatment, or an already present event that worsens either in intensity or frequency following the study treatment
| Participants | Cohort 1 | Cohort 2 | Cohort 3 and Cohort 5 | Cohort 4 and Cohort 6 | Cohort 7 | All Placebo |
|---|---|---|---|---|---|---|
| At least 1 TEAE | 3 | 5 | 11 | 12 | 6 | 14 |
| Related to study drug | 1 | 5 | 10 | 12 | 6 | 9 |
Collected over From the date of signing the consent form until Day 36. Non-serious events are listed at a 5% frequency threshold.
| Group | Deaths | Serious | Other |
|---|---|---|---|
| Cohort 1 | 0/6 (0%) | 0/6 (0%) | 3/6 (50%) |
| Cohort 2 | 0/5 (0%) | 0/5 (0%) | 5/5 (100%) |
| Cohort 3 and Cohort 5 | 0/12 (0%) | 0/12 (0%) | 11/12 (91.7%) |
| Cohort 4 and Cohort 6 | 0/12 (0%) | 0/12 (0%) | 12/12 (100%) |
| Cohort 7 | 0/6 (0%) | 0/6 (0%) | 6/6 (100%) |
| All Placebo | 0/21 (0%) | 0/21 (0%) | 11/21 (52.4%) |
| Event | Cohort 1 | Cohort 2 | Cohort 3 and Cohort 5 | Cohort 4 and Cohort 6 | Cohort 7 | All Placebo |
|---|---|---|---|---|---|---|
| Injection site reactionGeneral disorders | 1/6 | 5/5 | 10/12 | 12/12 | 6/6 | 6/21 |
| Injection site discolorationGeneral disorders | 0/6 | 0/5 | 0/12 | 0/12 | 5/6 | 0/21 |
| HeadacheNervous system disorders | 1/6 | 4/5 | 2/12 | 2/12 | 0/6 | 2/21 |
| Injection site painGeneral disorders | 0/6 | 0/5 | 1/12 | 4/12 | 0/6 | 0/21 |
| Audiogram abnormalInvestigations | 0/6 | 0/5 | 0/12 | 0/12 | 2/6 | 0/21 |
| Ear discomfortEar and labyrinth disorders | 0/6 | 0/5 | 1/12 | 3/12 | 0/6 | 0/21 |
| Injection site indurationGeneral disorders | 0/6 | 0/5 | 3/12 | 3/12 | 0/6 | 0/21 |
| Injection site hematomaGeneral disorders | 0/6 | 0/5 | 0/12 | 3/12 | 0/6 | 3/21 |
| NasopharyngitisInfections and infestations | 1/6 | 1/5 | 1/12 | 1/12 | 0/6 | 2/21 |
| SinusitisInfections and infestations | 0/6 | 1/5 | 0/12 | 0/12 | 0/6 | 0/21 |
| Age, Continuous(years) | Cohort 1 | Cohort 2 | Cohort 3 | Cohort 4 | Cohort 5 | Cohort 6 | Cohort 7 | All Placebo | Total |
|---|---|---|---|---|---|---|---|---|---|
| Mean | 41.2 ± 12.43 | 36.0 ± 8.69 | 37.7 ± 14.51 | 37.0 ± 11.26 | 37.8 ± 10.46 | 44.8 ± 11.14 | 33.5 ± 7.74 | 38.9 ± 11.16 | 38.5 ± 10.87 |
| Sex: Female, Male(Participants) | Cohort 1 | Cohort 2 | Cohort 3 | Cohort 4 | Cohort 5 | Cohort 6 | Cohort 7 | All Placebo | Total |
|---|---|---|---|---|---|---|---|---|---|
| Female | 5 | 0 | 3 | 2 | 1 | 0 | 3 | 7 | 21 |
| Male | 1 | 5 | 3 | 4 | 5 | 6 | 3 | 14 | 41 |
| Race (NIH/OMB)(Participants) | Cohort 1 | Cohort 2 | Cohort 3 | Cohort 4 | Cohort 5 | Cohort 6 | Cohort 7 | All Placebo | Total |
|---|---|---|---|---|---|---|---|---|---|
| American Indian or Alaska Native | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
| Asian | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
| Native Hawaiian or Other Pacific Islander | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
| Black or African American | 0 | 0 | 0 | 0 | 0 | 0 | 6 | 2 | 8 |
| White | 6 | 5 | 6 | 6 | 6 | 6 | 0 | 19 | 54 |
| More than one race | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
| Unknown or Not Reported | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
| Region of Enrollment(participants) | Cohort 1 | Cohort 2 | Cohort 3 | Cohort 4 | Cohort 5 | Cohort 6 | Cohort 7 | All Placebo | Total |
|---|---|---|---|---|---|---|---|---|---|
| Belgium | 6 | 5 | 6 | 6 | 6 | 6 | 0 | 18 | 53 |
| United States | 0 | 0 | 0 | 0 | 0 | 0 | 6 | 3 | 9 |
PDFs hosted by the registry, ClinicalTrials.gov.
Ran from Oct 2017 to primary completion in Jun 2019, 20 months.
Results were first posted in Mar 2021, 1 year 8 months after primary completion.
Of 14 phase 1 interventional studies under Genetic Diseases, Inborn, half reached primary completion within 6 months of starting (the median), counting those still running; a quarter within 2 and three quarters within 20. This study's 20 months is above that.
How these figures are worked out, and which studies are left out of them.
This study is completed, as verified in Feb 2021. You cannot join it, but the record below documents what was studied.
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Studies of the drug tested here: ELX-02
Eloxx Pharmaceuticals, Inc.