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A Phase 2A Clinical Trial to Assess the Safety and Tolerability of ERX1000 in Men and Women for the Treatment of Obesity.

6 maja 2026 zaktualizowane przez: ERX Pharmaceuticals

A Phase 2A, Randomized, Double-Blind, Placebo-Controlled, Clinical Study to Assess Efficacy, Safety and Tolerability of Orally Administered ERX1000 in Subjects With Obesity

The primary objective is to assess the safety and tolerability of oral dose ERX1000 in obese subjects.

Przegląd badań

Status

Jeszcze nie rekrutacja

Interwencja / Leczenie

Typ studiów

Interwencyjne

Zapisy (Szacowany)

80

Faza

  • Faza 2

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły

Akceptuje zdrowych ochotników

Nie

Opis

Inclusion Criteria:

  1. Able to comprehend and willing to sign an ICF and to abide by the study requirements.
  2. Male and female subjects ages 18-60 years, inclusive.
  3. BMI >30 to <50 kg/m2
  4. Stable body weight for 3 months (self-reported loss/gain <5%).
  5. Stable diet and/or nutritional lifestyle for 3 months prior to randomization.
  6. If a subject has current diagnosis of prediabetes, the following criteria must be met:

    1. Hemoglobin A1c (HbA1c) ≤6.4%
    2. Fasting glucose ≤125 mg/dL (≤6.94 mmol/L)
    3. No history of ketoacidosis or hyperosmolar coma
  7. Female subjects must not be pregnant or lactating. Nonpregnancy will be confirmed for all females by a urine pregnancy test conducted at Screening and at the Baseline Visit prior to enrollment into the study.

If of childbearing potential, the subject agrees to the use two of the following accepted contraceptive regimens from Screening to the first administration of the study drug, during the study, and for at least 30 days after the last dose of the study drug. Acceptable methods of contraception includes one of the following:

  1. Hormonal contraceptives (birth control pills, injectable/implant/insertable hormonal birth control products, transdermal patch), OR
  2. Intrauterine device (with or without hormones), AND
  3. Agrees to use a barrier method (e.g., male or female condom) during the study and for at least 30 days after the last dose of the study drug.

Exclusion Criteria:

  1. Poorly controlled severe psychiatric disorders (e.g., bipolar disorder, or major depressive disorder), recent (within 6 months) psychotic episodes, history of suicide attempts or suicidal ideation, or any other psychiatric disorders that the Investigator believes will interfere significantly with study compliance.
  2. Lifetime history of DSM-5 diagnosis of schizophrenia or schizoaffective disorder. Diagnosis of bipolar 1 disorder within the previous 2 years.
  3. History of any bleeding disorders, deep vein thrombosis (DVT), or thromboembolic disease.
  4. Current liver, renal, pulmonary, cardiac, oncologic, or gastrointestinal (GI) disease including:

    1. Significant cardiovascular disease including history of congestive heart failure (CHF), coronary artery disease, myocardial infarction (MI), second degree or greater heart block, prolonged time from electrocardiogram Q wave to the end of the T wave corresponding to electrical systole (QT) syndrome, or clinically significant arrhythmias.
    2. Fridericia-corrected QT interval (QTcF) >460 msec for males and QTcF >480 msec for females pre-dose on Day 1.
    3. Liver disease or liver function tests, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) >1.5 upper limit of normal (ULN), alkaline phosphatase (ALP) or serum bilirubin > ULN, or history of underlying liver disease including, hepatic cirrhosis, alcoholic hepatitis, or confirmed diagnosis of NASH; nonalcoholic fatty liver disease with qualifying LFTs will be allowed.
    4. History or presence of impaired renal function as indicated by clinically significant abnormal creatinine, blood urea nitrogen (BUN), or urinary constituents or moderate to severe renal dysfunction as defined by the Chronic Kidney Disease-Epidemiology Collaboration (CKD-EPI) equation (<60 mL/min/1.73m2).
  5. Type 1 diabetes mellitus or Type 2 diabetes mellitus or current or recent use of insulin (more than 1 week within 3 months prior to screening).
  6. Obesity induced by other endocrine disorders (e.g., Prader-Willi syndrome, Cushing's syndrome).
  7. Active autoimmune disease who are currently using or will likely require systemic glucocorticoid therapy in the next 6 months.
  8. Any previous surgical treatment or procedures with medical devices (such as insertion of lap band or gastric balloons) for obesity (excluding liposuction if performed > 1 year prior to screening).
  9. History of stomach or intestinal surgery or resection that would potentially alter absorption and/or excretion of orally administered drugs (uncomplicated appendectomy, cholecystectomy, and hernia repair > 6 months prior to Screening will be allowed).
  10. Uncontrolled endocrine disorders (e.g., Cushing syndrome, Addison's, Hashimoto's, hypothyroidism, hypogonadism).
  11. Clinically significant and abnormal screening hematology lab results or recurring infections, or if any of the following are observed regardless of the Investigator's assessment of clinical significance (laboratory tests may be repeated once for confirmation of out-of-range values):

    1. Hemoglobin <10 g/dL (<100 g/L)
    2. Absolute neutrophil count (ANC) <2000/mm3
    3. Platelets <135 x 109/L
    4. ALT or AST > 1.5 ULN
    5. GGT, ALP, total bilirubin, or INR > ULN
  12. Results of screening clinical laboratory tests (complete blood count [CBC] with differential and platelets, chemistry, and urinalysis profile) and electrocardiogram (ECG) outside normal range and considered to be clinically significant by the Investigator.
  13. Body weight of > 350 pounds (158.8 kilograms) due to weight limits of the DEXA scanner.
  14. Current use, or within the 30 days prior to screening, of the following atypical antipsychotic medications:

    1. Olanzapine
    2. Clozapine
    3. Quetiapine
  15. Subjects on the following systemic concomitant medications who have not been on stable dose (or stable weight-based dose), defined as no more than ±25% variation in dose, for at least 3 months prior to study entry:

    1. Vasopressin
    2. Thyroid hormone
    3. Testosterone
    4. Other hormone or hormone replacement therapies
    5. Anti-diabetes medications other than metformin (e.g., glucagon-like peptide-1 [GLP-1] receptor agonists, sodium-glucose linked transporter 2 (SGLT2) inhibitors, sulfonylureas)
    6. Modafinil
    7. Atypical anti-psychotics, other than those noted above
    8. Anti-depressives
    9. Attention deficit hyperactivity disorder (ADHD) medications
  16. Subjects on any prescription or over-the-counter anti-obesity agents in the 3 months prior to screening (e.g., Saxenda, Wegovy, Zepbound, Xenical, Acutrim, Qsymia, Adipex, compounded peptides).
  17. Chronic (>2 weeks) systemic glucocorticoid therapy (excluding topical, intraocular, intranasal, intra-articular, or inhaled preparations) within 1 month prior to study screening.
  18. Vital signs unstable, or with the following values:

    1. Systolic blood pressure >160 mm Hg
    2. Diastolic blood pressure >100 mm Hg
    3. Pulse rate >100 beats per minute (bpm)
  19. Recent (within the last year) and/or recurrent history of autonomic dysfunction (e.g., unexplained syncope or palpitations).
  20. Current or anticipated chronic use (more than 2 days) of narcotics or opiates.
  21. Significant history of abuse of drugs or solvents in the year before screening, or history of alcohol abuse in the past year before screening or currently drinks in excess of 21 units or servings per week.
  22. Participation in any clinical study with an investigational drug/device within 3 months.
  23. Positive result for human immunodeficiency virus (HIV), hepatitis B virus (HBV), or hepatitis C virus (HCV) prior to initiation of dosing with study drug.
  24. Serious adverse reaction or hypersensitivity to any drug which the Investigator believes is clinically significant and relevant to study participation.
  25. Significant blood loss or blood donation >500 mL within 3 months.
  26. Females who are pregnant, nursing, or intend to become pregnant during the study.
  27. Subjects who are planning or likely to undergo surgery during the course of the study.
  28. Subject is, in the opinion of the Investigator, not suitable to participate in the study (e.g., clinically significant illness in the 8 weeks before screening; unable to commit to study visits, etc.).

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Randomizowane
  • Model interwencyjny: Przydział równoległy
  • Maskowanie: Poczwórny

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Aktywny komparator: Treatment Arm
This arm will receive oral doses of ERX1000.
2mg tablet administered orally twice weekly.
Komparator placebo: Placebo Arm
This arm will receive placebo doses.
2mg Placebo tablet identical in appearance to 2mg ERX1000 tablet

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Ramy czasowe
Change in Body Weight of Participants from Baseline to Weeks 12 and 24
Ramy czasowe: From enrollment to the end of treatment at Week 24.
From enrollment to the end of treatment at Week 24.

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Number of subjects with Adverse Safety Parameters
Ramy czasowe: From enrollment to the end of study participation at Week 28.
The number of participants with (1) treatment related adverse events; (2) adverse changes in vital signs; (3) adverse changes in 12-lead ECG results; (4) adverse changs in safety laboratory results; (5) adverse changes as observed though physical examinations
From enrollment to the end of study participation at Week 28.
Change in Body Composition in Participants
Ramy czasowe: From enrollment to the end of treatment at Week 24.
(1) Change in % body fat by DEXA) from baseline to Weeks 12 and 24; (2) Change in BMI from baseline to Weeks 12 and 24; (3) Change in waist circumference from baseline to Weeks 12 and 24.
From enrollment to the end of treatment at Week 24.
Change in Metabolic Biomarkers
Ramy czasowe: From enrollment to the end of treatment at Week 24.
  1. Change in fasting lipid profile from baseline to Weeks 12 and 24: total cholesterol, low density lipoprotein (LDL), high density lipoprotein (HDL), and triglycerides;
  2. Change in plasma biomarkers from baseline to Weeks 12 and 24: leptin, insulin, glucose, and HbA1c
From enrollment to the end of treatment at Week 24.
Relationship Between Peak Drug Exposure and LFT Elevations
Ramy czasowe: From enrollment to Week 20.
Number of participants with elevated LFT results concurrent with peak concentration of ERX1000.
From enrollment to Week 20.

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Szacowany)

1 maja 2026

Zakończenie podstawowe (Szacowany)

1 maja 2027

Ukończenie studiów (Szacowany)

1 maja 2027

Daty rejestracji na studia

Pierwszy przesłany

30 kwietnia 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

30 kwietnia 2026

Pierwszy wysłany (Rzeczywisty)

6 maja 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

8 maja 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

6 maja 2026

Ostatnia weryfikacja

1 kwietnia 2026

Więcej informacji

Terminy związane z tym badaniem

Słowa kluczowe

Inne numery identyfikacyjne badania

  • ERX1000-O-100

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Tak

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

Badania kliniczne na ERX1000

Subskrybuj