A Phase 1 Study in Healthy Volunteers to Evaluate the Relative Bioavailability of ALG-055009 Formulations

NCT ID: NCT06959888

Last Updated: 2025-07-09

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 8 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-03-25
• Study Completion Date: 2025-05-16

Brief Summary

This is a phase 1 single dose, open-label, randomized, two-period, two-sequence, crossover study of ALG-055009 conducted in 1 cohort of healthy volunteers. The primary purpose of this study is to compare the single-dose pharmacokinetics of the 0.7 mg dose level of 2 types of soft gelatin capsule formulations of ALG-055009, Formulation 1 and Formulation 2, in approximately 8 healthy volunteers.

Conditions

Healthy Volunteer Study

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Sequence A

Single dose PO administration of 0.7 mg ALG-055009 (Formulation 1; Day 1), then a washout period of at least 7 days, followed by single dose PO administration of 0.7 mg ALG-055009 (Formulation 2; Day 8)

Group Type: EXPERIMENTAL

ALG-055009

Intervention Type: DRUG

Single PO dose of 0.7 mg ALG-055009 softgel capsule (formulation 1)

Single PO dose of 0.7 mg ALG-055009 softgel capsule (formulation 2)

Sequence B

Single dose PO administration of 0.7 mg ALG-055009 (Formulation 2; Day 1), then a washout period of at least 7 days, followed by single dose PO administration of 0.7 mg ALG-055009 (Formulation 1; Day 8)

Group Type: EXPERIMENTAL

ALG-055009

Intervention Type: DRUG

Single PO dose of 0.7 mg ALG-055009 softgel capsule (formulation 1)

Single PO dose of 0.7 mg ALG-055009 softgel capsule (formulation 2)

Interventions

ALG-055009

Single PO dose of 0.7 mg ALG-055009 softgel capsule (formulation 1)

Single PO dose of 0.7 mg ALG-055009 softgel capsule (formulation 2)

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Subject must sign an informed consent form (ICF) indicating that he or she understands that risks of purpose of and procedures required for, the study and is willing to participate in the study.

2. In the investigator's opinion, the subject is able to understand and comply with protocol requirements, instructions, and protocol stated restrictions and is likely to complete the study as planned.

3. Male or female between 18 and 65 years of age, extremes included.

4. Subjects must have a bod mass index (BMI) of 18.0 to 32.0 kg/m2, extremes included.

5. Female subjects must be either:

1. Post menopausal: A postmenopausal state is defined as no menses for at least 12 months without an alternative medical explanation . A high follicle-stimulating hormone (FSH) level in the postmenopausal range of >40 IU may be used to confirm a postmenopausal state in women not using hormonal contraception or hormonal replacement therapy (HRT).

OR

2. Permanently Sterile : Permanent sterilization methods include hysterectomy, bilateral salpingectomy, and bilateral oophorectomy.

OR

3. Woman of Childbearing Potential: They are only eligible if they and any non-sterile male sexual partners agree to use highly effective contraceptive therapy from the screening visit until at least 60 days after the last dose of study drug

6. Female subjects must have a negative pregnancy test at screening and Day-1.

7. Female subjects must not be pregnant, or breastfeeding, or planning to become pregnant or donate eggs from screening onward until 60 days after the last dose of study drug (or longer if dictated by local regulation).

8. Male subjects must agree to wear a condom during sexual intercourse and their female sexual partners should agree to use effective means of contraception. These contraceptive measures must be implemented, at a minimum, from the start of dosing until at least 90 days after the last dose.

9. Male subjects must have no plans to father a child or donate sperm while enrolled in this study or within 90 days after the last dose of study drug.

1. Heart rate between 40 and 100 beats per minute (bpm), extremes included;

2. QT interval corrected for heart rate (QTc) according to Fridericia's formula (QTcF) ≤450 ms (males) or ≤470 ms (females);

3. QRS interval ≤120 ms;

4. PR interval ≤110 to ≤220 ms;

5. In addition to fulfilling the above ECG criteria, ECG morphology must have no clinically significant abnormalities observed in the opinion of the Investigator.

11. Subjects must be deemed to be in good overall health by the investigator on the basis of a medical evaluation that reveals the absence of any clinically significant abnormality and includes a physical examination, medical history, vital signs, and the results of blood chemistry, blood coagulation and hematology tests, and a urinalysis performed at screening.

12. Subjects must be willing and able to adhere to the prior and concomitant medications requirements

Exclusion Criteria

Any potential subject who meets any of the following criteria will be excluded from participating in the study.

1. Subjects with any current or previous illness that, in the opinion of the investigator, might confound the results of the study or pose an additional risk in administering study drug to the subject or that could prevent, limit, or confound the protocol specified assessments or study results' interpretation. This may include, but is not limited to renal, cardiac, vascular, pulmonary, gastrointestinal, hepatologic, endocrine, neurologic, dermatologic, hematologic, rheumatologic, psychiatric, neoplastic, or metabolic disturbances.

2. Subjects with medical history or current evidence of a pituitary disorder or thyroid disorder.

3. Subjects with thyroid-stimulating hormone (TSH), free thyroxine (T4) or total triiodothyronine

4. Subjects with known sensitivity to thyroid medications

5. The laboratory values at screening are exclusionary:

1. ALT or AST > ULN

2. Total bilirubin > 1.2xULN, unless Gilbert's syndrome is suspected

6. Subjects with a past history of cardiac arrhythmias, risk factors for Torsade de Pointes syndrome (e.g., hypokalemia, family history of long QT syndrome ) or history or clinical evidence at screening of significant or unstable cardiac disease, such as: angina, congestive heart failure, myocardial infarction, diastolic dysfunction, significant arrhythmia.

7. History of unexplained syncope.

8. Subjects with current:

1. Hepatitis A virus infection (confirmed by hepatitis A antibody immunoglobulin M [IgM]).

2. Hepatitis B infection defined as presence of HBsAg or HBV core antibody.

3. Hepatitis C virus (HCV) infection (confirmed by HCV antibody and/or HCV RNA). Subjects who have been treated and achieved sustained virologic response ≥6 months prior to screening with HCV RNA <LLOQ, target not detected, remain eligible.

4. Human immunodeficiency virus type 1 (HIV-1) or HIV-2 infection (confirmed by antibodies) at screening.

5. Acute infection at the time of enrollment. If an acute infection is considered resolved prior to enrollment, the subject remains eligible.

9. Subjects who had major surgery (e.g., requiring general anesthesia) within 12 weeks before randomization, or will not have fully recovered from surgery, or have surgery planned during the time the subjects is expected to participate in the study, or within 4 weeks after the last dose of study drug

10. Subjects with a recent (within 1 year of randomization/enrollment) history of use of amphetamines, barbiturates, narcotic or other drugs of abuse/recreational drug use. Use of these drugs under physician supervision (e.g., prescription narcotics for known pain disorder) are not exclusionary. Cannabis use within 4 weeks of screening and during the study is exclusionary.

11. Excessive use of alcohol defined as regular consumption of ≥14 standard drinks/week for women and ≥21 standard drinks/week for men (Chalasani et al. 2018). For current definition of a standard drink, please refer to the National Institute on Alcohol Abuse and Alcoholism website (https://www.niaaa.nih.gov/what-standard-drink).

12. Unwilling to abstain from alcohol use for 48 hours prior to Day -1 through end of study follow up.

13. Positive results for urine drug screen or alcohol test at screening or Day -1.

15. Clinically significant abnormal vital signs (evaluated in the semi-recumbent [i.e., elevation of the head-to-bed at 30-45 degrees] or supine position after 5 minutes of rest), confirmed with retesting after at least 5 minutes of additional rest. Vital sign reference ranges to assess eligibility are as follows:

1. Systolic blood pressure: ≥90 to ≤140 mmHg

2. Diastolic blood pressure: ≥40 to ≤90 mmHg

3. Pulse rate: ≥40 to ≤100 beats per minute

16. Physical examination findings that are considered clinically significant and likely to adversely impact study conduct and/or interpretation are exclusionary.

17. Renal dysfunction [e.g., estimated creatinine clearance <90 mL/min/1.73 m2 at screening, calculated by the 2021 Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) formula (without correction for African ancestry)].

18. History of clinically significant drug allergy such as, but not limited to, sulfonamides or drug allergy witnessed in previous studies with experimental drugs.

19. Has taken or requires treatment with: any therapies as noted in Prior and Concomitant Medications (Section 6.10) and Special Precautions (Section 6.11) within 1 week or 5 half-lives (whichever is longer) before the planned first dose of study drug or during dosing; any Prohibited Medications (Appendix B) within 28 days or 5 half-lives (whichever is longer) before the planned first dose of study drug or during dosing.

20. Consumption of grapefruit, grapefruit juice, and Seville oranges within 14 days prior to study drug administration.

21. Consumption of apple or orange juice, citrus fruits, vegetables from the mustard green family (e.g., kale, broccoli, watercress, collard greens, kohlrabi, Brussels sprouts, mustard), and charbroiled meats within 7 days prior to study drug administration.

22. Consumption of any food or drink/beverage containing quinine (e.g., tonic, bitter lemon, bitter alcoholic beverages containing quinine) within 24 hours prior to study drug administration.

23. Received an unapproved investigational agent within 4 weeks (or 5 half-lives, whichever is longer) prior to enrollment.

24. Currently participating in another clinical or medical interventional research study.

25. Employee of the Sponsor, the Investigator or study site, with direct involvement in the proposed study or other studies under the direction of that Investigator or study site, as well as family members of the employees or the Investigator.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Aligos Therapeutics

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

PPD Austin CRU

Austin, Texas, United States

Countries

United States

Other Identifiers

ALG-055009-304

Identifier Type: -

Identifier Source: org_study_id