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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. Mai 2026 aktualisiert von: 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.

Studienübersicht

Status

Noch keine Rekrutierung

Studientyp

Interventionell

Einschreibung (Geschätzt)

80

Phase

  • Phase 2

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

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.).

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Vervierfachen

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Aktiver Komparator: Treatment Arm
This arm will receive oral doses of ERX1000.
2mg tablet administered orally twice weekly.
Placebo-Komparator: Placebo Arm
This arm will receive placebo doses.
2mg Placebo tablet identical in appearance to 2mg ERX1000 tablet

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
Change in Body Weight of Participants from Baseline to Weeks 12 and 24
Zeitfenster: From enrollment to the end of treatment at Week 24.
From enrollment to the end of treatment at Week 24.

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Number of subjects with Adverse Safety Parameters
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: From enrollment to Week 20.
Number of participants with elevated LFT results concurrent with peak concentration of ERX1000.
From enrollment to Week 20.

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

1. Mai 2026

Primärer Abschluss (Geschätzt)

1. Mai 2027

Studienabschluss (Geschätzt)

1. Mai 2027

Studienanmeldedaten

Zuerst eingereicht

30. April 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

30. April 2026

Zuerst gepostet (Tatsächlich)

6. Mai 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

8. Mai 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

6. Mai 2026

Zuletzt verifiziert

1. April 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Ja

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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