ClinicalTrials.gg
CompletedNCT03309605Updated Mar 16, 2021Results posted

Phase 1 Study of ELX-02 in Healthy Adult Subjects

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
Phase 1
Study type
Interventional
Enrollment
62
Allocation
Randomized
Ages
18 Years to 55 Years
Sex
All
01

Study summary

Phase 1 Multiple Ascending Dose Study in Normal Healthy Volunteers

Read the detailed description

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.

02

Conditions studied

  • Genetic Disease
  • Nonsense Mutation

Keywords

  • Translational read through
03

In context

Genetic Diseases, Inborn

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 →

Lead sponsor

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.

04

Who can participate

Ages eligible
18 Years to 55 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

Inclusion criteria: Subjects must meet all of the following inclusion criteria to be eligible for enrollment into the study:

  1. Be able and willing to provide written indicating that the subject has been informed of all pertinent aspects of the study.
  2. 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.

  3. Female subjects of non- must meet at least one of the following criteria:

    • Achieved status, defined as follows: cessation of regular menses for at least 12 consecutive months with no alternative pathological or physiological cause; post-menopausal status will be confirmed by a serum follicle-stimulating hormone level;
    • Have undergone a documented hysterectomy and/or bilateral oophorectomy;
    • Have medically confirmed ovarian failure. All other female subjects (including females with tubal ligations) will be considered to be of childbearing potential and may be enrolled if they have negative pregnancy tests at screening and admission day and agree to use a highly effective method of for 14 days before first study drug administration and 28 days after last study drug administration. Female subjects of childbearing potential must agree to undergo repeated pregnancy tests.
  4. Male subjects must be willing to use an effective method of contraception. They must agree to use a condom consistently and correctly, during the course of the study until 28 days after last study drug administration.
  5. Not using any prescription medication and dietary supplements within 30 days or 5 half lives (whichever is longer) prior to the first study drug administration, except for contraceptives - nor be taking any over-the-counter (OTC) herbal or medicinal products. As an exception, acetaminophen/paracetamol may be used at doses of ≤2 g/day.
  6. Non-smoking and no use of any tobacco or nicotine products (by declaration) for a period of at least 6 months prior to screening visit.
  7. Be on no medication with potential to impair renal function (e.g., non steroidal anti inflammatory [NSAID]s) or with ototoxic potential (e.g., quinine, salicylates, aminoglycosides).
  8. Normal renal function (glomular filtration rate >60 mL/min) based on creatinine plasma concentration and the Modification of Diet in Renal Disease () equation for estimated glomular filtration rate. Subjects with lower MDRD clearance can be included on the condition that they have a normal 24h (determined by a 24h urine collection).
  9. Negative (HIV), surface antigen (HBsAg), virus antibody (HCV Ab) serology tests at screening.
  10. No history of alcohol or DOA. Negative urine test for DOA and alcohol breath test at screening and Day -1.
  11. No personal history (or current) or hereditary hearing loss, persistent tinnitus, persistent vertigo, persistent imbalance and persistent unsteadiness.
  12. (BMI) of 19.0 to 30.0 kg/m2 (inclusive); and a total body weight >50.0 kg (110 lbs) and \<100.0 kg.

Exclusion criteria: Subjects with any of the following characteristics/conditions will not be included in the study:

  1. Subjects who are site staff members directly involved in the conduct of the study and their family members, site staff members otherwise supervised by the Investigator, or subjects who are the Sponsor employees directly involved in the conduct of the study.
  2. Concurrent participation or participation in another clinical trial within at least 5 tissue half-lives prior to dosing (calculated from the previous study's last dosing day). If the previous trial involved agents with delayed effects or prolonged metabolism, a 12 months interval is required.
  3. Evidence or history of clinically relevant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurologic, or allergic disease (including drug allergies). This includes any acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or investigational drug administration or may interfere with the interpretation of study results and, in the judgment of the Investigator, would make the subject inappropriate for entry into this study.
  4. Presence of mitochondrial mutations making subject susceptible to aminoglycoside toxicity.
  5. Subjects with any history of ear disease or surgeries, persistent dizziness or persistent tinnitus.
  6. 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.

  7. History of regular alcohol consumption exceeding 14 drinks/week for females or 21 drinks/week for males (1 drink = 150 mL of wine or 360 mL of beer or 45 mL of hard liquor) within 6 months of screening.
  8. Screening supine BP ≥ 140 mm Hg (systolic) or ≥ 90 mm Hg (diastolic), following at least 5 min of supine rest. If BP is ≥ 140 mm Hg (systolic) or ≥ 90 mm Hg (diastolic), the BP should be repeated two more times and the average of the three BP values should be used to determine the subject's eligibility.
  9. Screening supine 12-lead ECG demonstrating >450 msec for men and >470 msec for women, or a QRS interval >120 msec. If QTc or QRS exceed these limits, the ECG should be repeated two more times and the average of the three QTc or QRS values should be used to determine the subject's eligibility.
  10. Subjects with ANY abnormalities in clinical laboratory tests at screening, considered by the study physician as clinically relevant. In particular, subjects with (ALT), aspartate aminotransferase (AST), serum creatinine and total ≥ 1.5 will be excluded.
  11. Pregnant or breastfeeding female subjects.
  12. Subjects who donated blood or received blood or plasma derivatives in the three months preceding study drug administration.
  13. Unwilling or unable to comply with all scheduled visits, treatment plan, laboratory tests and other study procedures and the restrictions described in this protocol.
  14. Known relevant allergy to any drug and/or aminoglycosides.
  15. Subjects with an inability to communicate well with the Investigators and CPU staff (e.g., language problem, poor mental development).
  16. Subjects with visual impairment or inability to read and comprehend the DHI and THI scales.
  17. Subjects with any acute medical situation (e.g., acute infection) within 48 hours of study start, which is considered of significance by the Investigator.
Terms in these criteria, in plain language(17)

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.

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.

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.

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.

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.

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).

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
62 participants (actual)

Study arms

  • Placebo comparator
    Placebo Comparator Arm

    Placebo

    Drug: Placebo

  • Experimental
    ELX-02

    ELX-02

    Drug: ELX-02

Interventions

  • DrugELX-02

    ELX-02 is a synthetic, designer eukaryotic ribosomal specific glycoside (ERSG) optimized as a translational read-through drug

  • DrugPlacebo

    Placebo

06

What researchers measure

Primary outcomes

  1. 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

  2. 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

  3. 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

  4. 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

  5. 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

  6. 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

  7. 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

  8. 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

  9. Pharmacokinetic Parameter - Plasma Rac(AUC24h)

    Accumulation ratio, calculated as AUC24h Day29/AUC24h Day 1

    Time frame: Day 1 and Day 24 hr

  10. Pharmacokinetic Parameter - Plasma RAC(Cmax)

    Accumulation ratio, calculated as Cmax Day29/Cmax Day 1

    Time frame: Day 1 and Day 29

  11. 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

  12. 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

  13. 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

  14. 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

  15. Urine Pharmacokinetics Parameter - Fe12h Day 1

    Percent of dose excreted (Fe) in urine on Day 1

    Time frame: 12 hours

  16. 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

  17. Urine Pharmacokinetics Parameter - CLR24h on Day 1

    Renal clearance on Day 1 (CLR=Ae24h/plasmaAUC24h)

    Time frame: 24 hours

  18. Urine Pharmacokinetics Parameter - CLR24h

    Renal clearance on Day 29 (CLR=Ae24h/plasmaAUC24h)

    Time frame: 24 h

Secondary outcomes

  1. 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

07

Results

Posted Mar 16, 2021

Participant flow

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.

Participant flow — Overall Study
MilestoneCohort 1Cohort 2Cohort 3Cohort 4Cohort 5Cohort 6Cohort 7All Placebo
Started656666621
Completed656556319
Not completed00011032
Withdrew: Adverse event00010021
Withdrew: Withdrawal by subject00001011

Outcome measures

PrimaryPharmacokinetic 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
Reported as:
Geometric mean · ng*h/mL
Pharmacokinetic Parameters - Plasma AUC0-24
ng*h/mLCohort 1Cohort 2Cohort 3 and Cohort 5Cohort 4 and Cohort 6Cohort 7
Pharmacokinetic Parameters - Plasma AUC0-241105.126 ± 15.2613125.484 ± 13.83611018.22 ± 12.43628235.823 ± 16.25561906.528 ± 20.455
PrimaryPharmacokinetic 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
Reported as:
Geometric mean · ng*h/mL
Pharmacokinetic Parameters- Plasma AUC0-24
ng*h/mLCohort 1Cohort 2Cohort 3 and Cohort 5Cohort 4 and Cohort 6Cohort 7
Pharmacokinetic Parameters- Plasma AUC0-241215.098 ± 15.4313109.978 ± 16.60110847.306 ± 14.09829651.700 ± 23.22354749.370 ± 13.770
PrimaryPharmacokinetic 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
Reported as:
Geometric mean · ng/mL
Pharmacokinetic Parameters - Plasma Cmax
ng/mLCohort 1Cohort 2Cohort 3 and Cohort 5Cohort 4 and Cohort 6Cohort 7
Pharmacokinetic Parameters - Plasma Cmax284.710 ± 21.0601003.266 ± 5.7662880.233 ± 11.6477721.256 ± 6.38715912.090 ± 17.265
PrimaryPharmacokinetic 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
Reported as:
Geometric mean · ng/mL
Pharmacokinetic Parameters - Plasma Cmax
ng/mLCohort 1Cohort 2Cohort 3 and Cohort 5Cohort 4 and Cohort 6Cohort 7
Pharmacokinetic Parameters - Plasma Cmax342.779 ± 12.021961.448 ± 7.4602806.966 ± 16.4037852.172 ± 12.34215435.789 ± 13.872
PrimaryPharmacokinetic 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
Reported as:
Geometric mean · ng*hr/mL
Pharmacokinetic Parameter - Plasma AUC0-inf
ng*hr/mLCohort 1Cohort 2Cohort 3 and Cohort 5Cohort 4 and Cohort 6Cohort 7
Pharmacokinetic Parameter - Plasma AUC0-inf1107.272 ± 15.3453127.964 ± 13.89811036.305 ± 12.63128335.680 ± 16.46862142.763 ± 20.712
PrimaryPharmacokinetic 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
Reported as:
Geometric mean · ng*h/mL
Pharmacokinetic Parameter - Plasma AUC0-inf
ng*h/mLCohort 1Cohort 2Cohort 3 and Cohort 5Cohort 4 and Cohort 6Cohort 7
Pharmacokinetic Parameter - Plasma AUC0-inf1216.448 ± 15.4283114.486 ± 16.70410862.927 ± 14.23929778.143 ± 23.46954933.538 ± 13.979
PrimaryPharmacokinetic 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
Reported as:
Median · hour
Pharmacokinetic Parameter - Plasma Tmax
hourCohort 1Cohort 2Cohort 3 and Cohort 5Cohort 4 and Cohort 6Cohort 7
Pharmacokinetic Parameter - Plasma Tmax1.00 (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)
PrimaryPharmacokinetic 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
Reported as:
Median · hour
Pharmacokinetic Parameter Plasma - Tmax
hourCohort 1Cohort 2Cohort 3 and Cohort 5Cohort 4 and Cohort 6Cohort 7
Pharmacokinetic Parameter Plasma - Tmax1.00 (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)
PrimaryPharmacokinetic Parameter - Plasma Rac(AUC24h)

Accumulation ratio, calculated as AUC24h Day29/AUC24h Day 1

Time frame:
Day 1 and Day 24 hr
Reported as:
Geometric mean · Ratio
Pharmacokinetic Parameter - Plasma Rac(AUC24h)
RatioCohort 1Cohort 2Cohort 3 and Cohort 5Cohort 4 and Cohort 6Cohort 7
Pharmacokinetic Parameter - Plasma Rac(AUC24h)1.093 ± 7.4970.995 ± 6.6220.984 ± 7.8921.056 ± 14.1610.911 ± 13.377
PrimaryPharmacokinetic Parameter - Plasma RAC(Cmax)

Accumulation ratio, calculated as Cmax Day29/Cmax Day 1

Time frame:
Day 1 and Day 29
Reported as:
Geometric mean · Ratio
Pharmacokinetic Parameter - Plasma RAC(Cmax)
RatioCohort 1Cohort 2Cohort 3 and Cohort 5Cohort 4 and Cohort 6Cohort 7
Pharmacokinetic Parameter - Plasma RAC(Cmax)1.217 ± 15.2780.958 ± 7.4290.976 ± 12.4011.018 ± 15.4130.941 ± 1.262
PrimaryUrine 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
Reported as:
Geometric mean · mg
Urine Pharmacokinetics Parameter - Ae72h
mgCohort 1Cohort 2Cohort 3 and Cohort 5Cohort 4 and Cohort 6Cohort 7
Urine Pharmacokinetics Parameter - Ae72h6.702 ± 16.72115.177 ± 8.52458.270 ± 20.046160.665 ± 11.622332.467 ± 18.102
PrimaryUrine 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
Reported as:
Geometric mean · mg
Urine Pharmacokinetics Parameter - Ae72h
mgCohort 1Cohort 2Cohort 3 and Cohort 5Cohort 4 and Cohort 6Cohort 7
Urine Pharmacokinetics Parameter - Ae72h6.331 ± 28.50515.021 ± 9.18966.354 ± 15.505162.609 ± 12.742399.302 ± 14.863
PrimaryUrine 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
Reported as:
Geometric mean · mg/h
Urine Pharmacokinetic Parameter - Rmax
mg/hCohort 1Cohort 2Cohort 3 and Cohort 5Cohort 4 and Cohort 6Cohort 7
Urine Pharmacokinetic Parameter - Rmax1.846 ± 30.5614.759 ± 6.70616.132 ± 15.54041.587 ± 21.20069.304 ± 13.495
PrimaryUrine 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
Reported as:
Geometric mean · mg/h
Urine Pharmacokinetic Parameter - Rmax
mg/hCohort 1Cohort 2Cohort 3 and Cohort 5Cohort 4 and Cohort 6Cohort 7
Urine Pharmacokinetic Parameter - Rmax1.950 ± 37.9385.028 ± 15.87518.327 ± 23.86240.607 ± 18.38989.796 ± 14.725
PrimaryUrine Pharmacokinetics Parameter - Fe12h Day 1

Percent of dose excreted (Fe) in urine on Day 1

Time frame:
12 hours
Reported as:
Geometric mean · percentage of drug excreted
Urine Pharmacokinetics Parameter - Fe12h Day 1
percentage of drug excretedCohort 1Cohort 2Cohort 3 and Cohort 5Cohort 4 and Cohort 6Cohort 7
Urine Pharmacokinetics Parameter - Fe12h Day 179.572 ± 10.03079.440 ± 6.17876.028 ± 17.40389.639 ± 9.22783.362 ± 5.495
PrimaryUrine Pharmacokinetics Parameter - Fe 12h on Day 29

Percent of dose excreted (Fe) in urine on Day 29

Time frame:
12 h on Day 29
Reported as:
Geometric mean · percentage of drug excreted
Urine Pharmacokinetics Parameter - Fe 12h on Day 29
percentage of drug excretedCohort 1Cohort 2Cohort 3 and Cohort 5Cohort 4 and Cohort 6Cohort 7
Urine Pharmacokinetics Parameter - Fe 12h on Day 2976.095 ± 14.87478.398 ± 3.61588.130 ± 15.21888.914 ± 4.15794.219 ± 7.407
PrimaryUrine Pharmacokinetics Parameter - CLR24h on Day 1

Renal clearance on Day 1 (CLR=Ae24h/plasmaAUC24h)

Time frame:
24 hours
Reported as:
Geometric mean · L/h
Urine Pharmacokinetics Parameter - CLR24h on Day 1
L/hCohort 1Cohort 2Cohort 3 and Cohort 5Cohort 4 and Cohort 6Cohort 7
Urine Pharmacokinetics Parameter - CLR24h on Day 15.871 ± 22.6454.823 ± 9.8345.251 ± 19.1355.653 ± 22.9595.331 ± 16.660
PrimaryUrine Pharmacokinetics Parameter - CLR24h

Renal clearance on Day 29 (CLR=Ae24h/plasmaAUC24h)

Time frame:
24 h
Reported as:
Geometric mean · L/h
Urine Pharmacokinetics Parameter - CLR24h
L/hCohort 1Cohort 2Cohort 3 and Cohort 5Cohort 4 and Cohort 6Cohort 7
Urine Pharmacokinetics Parameter - CLR24h5.152 ± 29.2344.784 ± 10.8286.068 ± 17.2005.435 ± 28.5217.239 ± 7.903
SecondaryNumber 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
Reported as:
Count of participants · Participants
Number of Patients Experiencing at Least One Treatment-Emergent Adverse Events (TEAEs)
ParticipantsCohort 1Cohort 2Cohort 3 and Cohort 5Cohort 4 and Cohort 6Cohort 7All Placebo
At least 1 TEAE351112614
Related to study drug15101269

Adverse events

Collected over From the date of signing the consent form until Day 36. Non-serious events are listed at a 5% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Cohort 10/6 (0%)0/6 (0%)3/6 (50%)
Cohort 20/5 (0%)0/5 (0%)5/5 (100%)
Cohort 3 and Cohort 50/12 (0%)0/12 (0%)11/12 (91.7%)
Cohort 4 and Cohort 60/12 (0%)0/12 (0%)12/12 (100%)
Cohort 70/6 (0%)0/6 (0%)6/6 (100%)
All Placebo0/21 (0%)0/21 (0%)11/21 (52.4%)
Most frequent other events
Showing 10 of 35
Most frequent other events
EventCohort 1Cohort 2Cohort 3 and Cohort 5Cohort 4 and Cohort 6Cohort 7All Placebo
Injection site reactionGeneral disorders1/65/510/1212/126/66/21
Injection site discolorationGeneral disorders0/60/50/120/125/60/21
HeadacheNervous system disorders1/64/52/122/120/62/21
Injection site painGeneral disorders0/60/51/124/120/60/21
Audiogram abnormalInvestigations0/60/50/120/122/60/21
Ear discomfortEar and labyrinth disorders0/60/51/123/120/60/21
Injection site indurationGeneral disorders0/60/53/123/120/60/21
Injection site hematomaGeneral disorders0/60/50/123/120/63/21
NasopharyngitisInfections and infestations1/61/51/121/120/62/21
SinusitisInfections and infestations0/61/50/120/120/60/21

Baseline characteristics

Age, Continuous
Age, Continuous(years)Cohort 1Cohort 2Cohort 3Cohort 4Cohort 5Cohort 6Cohort 7All PlaceboTotal
Mean41.2 ± 12.4336.0 ± 8.6937.7 ± 14.5137.0 ± 11.2637.8 ± 10.4644.8 ± 11.1433.5 ± 7.7438.9 ± 11.1638.5 ± 10.87
Sex: Female, Male
Sex: Female, Male(Participants)Cohort 1Cohort 2Cohort 3Cohort 4Cohort 5Cohort 6Cohort 7All PlaceboTotal
Female5032103721
Male15345631441
Race (NIH/OMB)
Race (NIH/OMB)(Participants)Cohort 1Cohort 2Cohort 3Cohort 4Cohort 5Cohort 6Cohort 7All PlaceboTotal
American Indian or Alaska Native000000000
Asian000000000
Native Hawaiian or Other Pacific Islander000000000
Black or African American000000628
White65666601954
More than one race000000000
Unknown or Not Reported000000000
Region of Enrollment
Region of Enrollment(participants)Cohort 1Cohort 2Cohort 3Cohort 4Cohort 5Cohort 6Cohort 7All PlaceboTotal
Belgium65666601853
United States000000639
08

Study locations

1 site
  • SGS Life Sciences, Clinical Pharmacology Unit
    Antwerp, Belgium
09

References and documents

Publications

  • Leubitz A, Vanhoutte F, Hu MY, Porter K, Gordon E, Tencer K, Campbell K, Banks K, Haverty T. A Randomized, Double-Blind, Placebo-Controlled, Multiple Dose Escalation Study to Evaluate the Safety and Pharmacokinetics of ELX-02 in Healthy Subjects. Clin Pharmacol Drug Dev. 2021 Aug;10(8):859-869. doi: 10.1002/cpdd.914. Epub 2021 Jan 19. PubMed 33465285 ↗

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

10

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

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.

Registered
Oct 10, 2017
First posted
Oct 13, 2017
StartActual
Oct 11, 2017
Primary completionActual
Jun 17, 2019
CompletionActual
Jul 17, 2019
Results first posted
Mar 16, 2021
Last update
Mar 16, 2021
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Mar 16, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT03309605
Lead sponsor
Eloxx Pharmaceuticals, Inc.
Collaborators
SGS Life Sciences, a division of SGS Belgium NV
Responsible party
Sponsor
First posted
Oct 13, 2017
Start date
Oct 11, 2017
Primary completion
Jun 17, 2019
Completion
Jul 17, 2019
Results posted
Mar 16, 2021
Last update
Mar 16, 2021

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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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

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