NCT05876312Toboroz1/2. fázis
Safety, Tolerability, PK and PD of ADX-038 in Healthy Participants and Paroxysmal Nocturnal Hemoglobinuria (PNH) Patients
A Phase 1, Randomized, Double Blind, Placebo-Controlled, Single Ascending Dose Study in Healthy Participants Followed by a Phase 2a Open Label Study in Participants With PNH and Residual Anemia to Evaluate the Safety, Tolerability, PK and PD of ADX-038
Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. jún. 16.
Rövid összefoglaló (regiszter, angolul)
The first-in-human Phase 1/Phase 2a study described herein will evaluate the safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of ADX-038 in both healthy participants (HP) and in patients with paroxysmal nocturnal hemoglobinuria (PNH).
- Állapot (regiszter)
- Toboroz
- Fázis (regiszter)
- 1/2. fázis
- Vizsgálattípus
- Beavatkozással járó
- Résztvevők száma
- 50 (tervezett)
- Első benyújtás
- 2023. máj. 17.
- Kezdés
- 2023. aug. 7.
- Elsődleges befejezés
- 2028. márc. 31.
- Fő szponzor
- ADARx Pharmaceuticals, Inc.
- NCT-szám
- NCT05876312
Mit vállalsz
- Vizsgálat típusa: Beavatkozással járó · 1/2. fázis
- Tervezett résztvevők: 50
- 2023. aug. 7. és az elsődleges befejezés (2028. márc. 31.) között
- 4 helyszín, 2 országban
- Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket
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- Phase 1 Key Inclusion Criteria
- 18 to 55 years of age
- Participants who are healthy as determined by medical evaluation
- History of recent meningococcal, pneumococcal and Haemophilus influenzae type B vaccinations or willing to be vaccinated
- Screening tests negative for illicit drug, nicotine, and alcohol use
- Phase 1 Key Exclusion Criteria
- History of any significant medical conditions, except for completely excised non-melanoma skin cancer or low grade cervical intraepithelial neoplasia without evidence of recurrence within the prior 3 months
- Any viral, bacterial, parasitic, or fungal infection within the prior 30 days
- Frequent respiratory, nasopharyngeal or ear infections (more than 5 infections per year)
- History of environmental exposure or sick contact that increase the risk of meningococcal, pneumococcal and/or Haemophilus influenza type B infections
- Complement deficiency or immunodeficiency syndrome
- Major surgery or significant traumatic injury within the prior 3 months
- History of anaphylaxis or hypersensitivity reactions
- History of penicillin allergy
- History of splenectomy
- History of alcohol abuse or illicit drug use
- Donated plasma within the prior 7 days
- Donated blood or loss more than 400 milliliters of blood (excluding blood volume drawn at screening) within the prior 90 days
- Screening estimated creatinine clearance of less than 60 milliliters per minute
- Screening hematology, serum chemistry, or coagulation parameters that are outside the normal range
- Screening vital signs that are abnormal per protocol specification
- Screening electrocardiogram findings that are clinically significant
- Pregnant or lactating females
- Use of prescription (except for contraceptives and study-related prophylactic antibiotics) or over-the counter medications (except for paracetamol or ibuprofen) or vitamins/supplements within the prior 7 days
- Use of medications that may reduce the effectiveness of hormonal contraceptives within the prior 28 days
- Use of an investigational therapeutics within the prior 30 days or within the expected washout (at least 5 half-lives)
- Unwilling or unable to adhere to study-related prophylactic antibiotics requirements
- Phase 2a Key Inclusion Criteria
- at least 18 years of age
- Diagnosis of paroxysmal nocturnal hemoglobinuria based on documented clone size
- Hemoglobin concentration of less than 12 gram per deciliter
- History of recent meningococcal, pneumococcal and Haemophilus influenzae type b vaccinations or willing to be vaccinated
- On a stable anti-C5 regimen for greater than or equal to 12 weeks prior to Day 1
- Phase 2a Key Exclusion Criteria
- Any viral, bacterial, parasitic, or fungal infection within the prior 14 days
- HIV, active hepatitis C or hepatitis B infection
- History of meningococcal or tuberculosis infection
- History of malignancy in the past 5 years, except for completely excised non-melanoma skin cancer or low grade cervical intraepithelial neoplasia with no evidence of recurrence within the prior 3 months
- Complement deficiency syndrome
- History of hematopoietic stem cell transplantation
- History of splenectomy
- Inflammatory bowel disease, systemic lupus erythematosus, rheumatoid arthritis, or chronic liver disease
- Clinically significant and uncontrolled medical conditions including, but not limited to, thromboembolic disease, acute coronary syndrome, and diabetes
- Pregnant or lactating females
- Use of an investigational therapeutics within the prior 30 days or within the expected washout period (at lest 5 half-lives)
- Abstain from alcohol consumption for 48 hrs before day of dosing and restrict to no more than an average of 14 standard drinks per week
Életkor a regiszterben: 18 év – - · Nem: nők és férfiak · Egészséges önkénteseket is fogad
Helyszínek (4)
Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.
| Helyszín | Város | Ország | Helyszín állapota |
|---|---|---|---|
| Nucleus Network Brisbane | Brisbane | Ausztrália | Befejeződött |
| Peter MacCallum Cancer Centre | Melbourne | Ausztrália | Befejeződött |
| Royal Melbourne Hospital | Parkville | Ausztrália | Toboroz |
| Richmond Pharmacology Ltd | London | Egyesült Királyság | Befejeződött |
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