Safety, Tolerability, and Immunogenicity of ALFQ in a HIV Vaccine Containing A244 and B.65321 in Healthy Adults

Phase 1

Recruiting

• Conditions: AIDS Virus; Human Immunodeficiency Virus (HIV)
• Interventions: Biological: A244; Biological: B.63521; Biological: 200μg ALFQ; Biological: 100μg ALFQ; Biological: 50μg ALFQ

• Registration Number: NCT05423418
• Lead Sponsor: U.S. Army Medical Research and Development Command

Brief Summary

This study will evaluate the safety and tolerability (including reactogenicity) of candidate vaccine A244/B.63521 with Army Liposome Formulation (ALF) mixed with the saponin QS-21(Quillaja saponaria-21) (ALFQ) adjuvant. The purpose of this phase I randomized, double-blind clinical trial is to optimize vaccine adjuvant ALFQ dosing by assessing safety, reactogenicity, and immunogenicity. Safety and tolerability will be assessed with both clinical and laboratory monitoring. Sixty human immunodeficiency virus (HIV) negative participants will be enrolled to one of three arms. Vaccinations via intramuscular (IM) injection will occur at months 0, 1, and 2. All participants will receive A244 and B.63521 (300 micrograms of each). In addition, Arm 1 will receive 200 micrograms of ALFQ. Arm 2 will receive 100 micrograms of ALFQ. Arm 3 will receive 50 micrograms of ALFQ.

Detailed Description

The purpose of this Phase I randomized, double-blind clinical trial is to optimize ALFQ dosing. Safety will be assessed through the frequency of the overall and specific post-vaccination reactions. Blood will be collected to assess humoral, cell-mediated, and innate immune responses.

Healthy adults not living with HIV who are available for 14 months will be enrolled. A total of 60 participants will be enrolled to one of three arms, each comprised of 20 candidate vaccine recipients. Each arm will receive identical doses of A244 and B.63521 (300 micrograms of each). In addition, Arm 1 will receive 200 micrograms of ALFQ. Arm 2 will receive 100 micrograms of ALFQ. Arm 3 will receive 50 micrograms of ALFQ. The safety, reactogenicity, and immunogenicity will then be compared among the three arms to determine the optimal dose of ALFQ.

All vaccinations will be split into 2 half doses which will both be administered intramuscularly (IM) into the same deltoid muscle. Vaccinations will occur at months 0, 1, and 2. The second vaccination will be administered into the contralateral deltoid at study month 1 compared to the first vaccination at study month 0. The third vaccination at study month 2 will be administered into the same deltoid as the first vaccination at study month 0. Participants will be followed for 12 months following the last study vaccination. Safety and tolerability will be assessed with both clinical and laboratory monitoring. Vaccine- related reactions will be observed and solicited for 30 minutes post-vaccination and with the aid of a diary card and interview of participants during the 14 days post vaccination.

The information gained from the review of the diary card and the interview with the participants will be documented in the clinical study chart. In addition, adverse events (AEs) will be documented at each clinical encounter. AEs will be graded for seriousness, severity, and relationship to the investigational product.

Study Timeline

• Study First Submitted: 2022-06-06
• Study First Submitted QC: 2022-06-14
• Study First Posted: 2022-06-21
• Study Start: 2022-08-29
• Status Verified: 2023-06
• Last Update Submitted: 2023-06-15
• Last Update Posted: 2023-06-18
• Primary Completion: 2023-10-23
• Study Completion: 2028-10-23

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

1. Healthy adults between the ages 18-55 years (inclusive)

2. Must be at low risk for HIV infection per investigator assessment and using the study risk assessment tool.

3. Able and willing to provide written, informed consent

4. Able and willing to comply with all research requirements, in the opinion of the Investigator

5. Agreement to refrain from blood donation during the course of the study

6. Minimum body weight of 110 pounds (lbs) (50kg)

7. Laboratory Criteria within 30 days before enrollment:

   1. Hemoglobin ≥ 12.0 g/dL for women; ≥ 12.5 g/dL for men
   2. White Blood Cell count = 3,500-10,800 cells/mm3
   3. Platelets ≥140,000/mm3 and ≤ 450,000/mm3
   4. Alanine aminotransferase (ALT; SGPT) <1.25 x Upper Limit of Normal (ULN)
   5. Serum creatinine ≤ 1.25 x institutional upper limit of the reference range
   6. Negative HIV testing (HIV Ab / antigen 4th generation screen with reflex confirmatory RNA testing)
   7. Negative HBsAg and hepatitis C antibody testing Note: As above, Grade 1 lab abnormalities detected on screening may be repeated at PI discretion. Persistent Grade 1 abnormalities that are felt to represent the non-pathologic baseline for the subject will be documented before a subject is enrolled in the trial and are allowable per discretion of the PI.

8. Birth control requirements:

   All participants assigned female at birth must meet one of the following 2 criteria:

   1. No reproductive potential due to post-menopausal status (12 months of natural [spontaneous] amenorrhea) or hysterectomy, bilateral oophorectomy, or tubal ligation
   2. People of childbearing potential should agree to practice highly effective contraception at least 30 days before enrollment and through 3 months post-last vaccination, using one of the following methods: condoms (male or female) with spermicide; diaphragm, or cervical cap with spermicide; intrauterine device; contraceptive pills, patch, injection, intravaginal ring or other FDA-approved contraceptive method; male partner has previously undergone a vasectomy; abstinence
   3. All participants are encouraged to engage in safe sex practices to prevent HIV acquisition

9. For all participants assigned female at birth, except those with a history of hysterectomy or bilateral oophorectomy, a negative β-human chorionic gonadotropin (HCG) pregnancy test (urine) on the day of enrollment and each vaccination day is required. Because tubal ligations have a failure rate that is not insignificant, and because 12 months of spontaneous amenorrhea can be a result of polycystic ovarian syndrome and does not completely preclude pregnancy, a negative β- HCG pregnancy test at enrollment and on each vaccination day is also required for participants assigned female at birth with a history of either of these).

10. No plans to travel outside the Washington DC metro area (DC, Maryland, and Virginia) that would prevent compliance with planned study visits

11. Test of Understanding (TOU) (minimum passing score of 80% with 2 attempts permitted)

Exclusion Criteria

1. Receipt of any investigational HIV vaccine or investigational adjuvant

2. Received an investigational product in the 30 days before enrollment, or planned to receive during the study period. This does not include products with emergency use authorization.

3. Concurrent participation in another clinical research study

4. Any serious medical illness or condition

5. Receipt of immunoglobulins or blood products within 3 months before enrollment

6. Any history of anaphylaxis or allergy to study product

7. History of sickle cell trait or disease

8. Pregnancy, lactation, or intention to become pregnant during the study

9. History of active/recent cancer still within treatment or active surveillance follow-up (except basal cell carcinoma of the skin and cervical carcinoma in situ). Treated/resolved cancers with no likelihood of recurrence may be deemed acceptable at Principal Investigator (PI) discretion.

10. History of autoimmune disease

11. History of Potentially Immune-Mediated Medical Conditions (PIMMCs)

12. Suspected or known current alcohol or drug abuse as defined by an alcohol intake of greater than 3 drinks a day on average for a man, and greater than 2 drinks a day on average for a woman

13. Any other significant disease, disorder or finding which may significantly increase the risk to the volunteer because of participation in the study, affect the ability of the volunteer to give informed consent, participate in the study, or impair interpretation of the study data, in the opinion of the Investigator

14. History of splenectomy

15. History of confirmed or suspected immunodeficiency

16. History of hereditary angioedema (HAE) acquired angioedema (AAE), or idiopathic forms of angioedema

17. History of asthma that is unstable or required emergent care, urgent care, hospitalization, or intubation during the past 2 years

18. History of diabetes mellitus (type I or II), with the exception of gestational diabetes

19. History of thyroid disease (except for well controlled hypothyroidism)

20. History of idiopathic urticaria within the past year

21. History of hypertension that is not well controlled by medication or that is persistently greater than 140/95 at screening

22. History of bleeding disorder diagnosed by a doctor (e.g., factor deficiency, coagulopathy, or platelet disorder requiring special precautions) or significant bruising or bleeding difficulties with IM injections or blood draws

23. History of chronic or active neurologic disease to include seizure disorder and chronic migraine headaches. Exceptions are: i) childhood febrile seizures, or ii) seizures secondary to alcohol withdrawal more than 3 years ago

24. Subjects receiving any of the following substances:

    1. Systemic immunosuppressive medications or cytotoxic medications within 12 weeks before enrollment [with the exception of a short course of corticosteroids (≤ 14 days duration or a single injection) for a self-limited condition at least 2 weeks before enrollment; inhaled, intranasal or topical steroids are not considered exclusionary
    2. Treatment with known immunomodulators including allergy immunotherapy (other than nonsteroidal anti-inflammatory drugs [NSAIDs] or stable maintenance immunotherapy (doses not in the process of being increased), at the discretion of the Protocol Safety Review Team (PSRT)) for any reason
    3. Live attenuated vaccines within 30 days before initial study vaccine administration
    4. Medically indicated subunit, messenger ribonucleic acid (mRNA), or killed vaccines, e.g., influenza, pneumococcal, vaccines with Quillaja saponaria-21 (QS-21) as an adjuvant, or allergy treatment with antigen injections, planned for administration 14 days before or after study vaccine administration

25. History of arthritis diagnosis other than osteoarthritis

26. History of other diagnosed rheumatoid disorders

27. Has an acute illness or temperature ≥38.0 degrees Celsius (C)/100.4 degrees Fahrenheit (F) on any study injection day or within 48 hours of planned study injection.

Note: Participants will not be excluded from further consideration for enrollment and study injections. Volunteers with fever or an acute illness on the day of study injection or in the 2 days before the study injection may be re-assessed by a study physician for resolution of the condition and enrolled and receive the study injection so long as the injection is within allowable windows. Military personnel will be excluded from participation in this study, regardless of leave status due to the potential for a false-positive HIV test result on mandatory HIV testing. This could have adverse effects on deployment status.

Final evaluation of eligibility will be based on the medical judgment of the investigator based on his/her medical and research experience.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SEQUENTIAL

Arm && Interventions

Group	Intervention	Description
A244/B.63521 + 200 μg of ALFQ adjuvant	B.63521	Arm 1: An injection containing 300 μg A244 plus 300 μg B.63521 with 200 μg of ALFQ adjuvant will be administered as an IM injection into the deltoid muscle at visits 1, 3, and 5 (corresponding to Day 1, Day 29, and Day 57).
A244/B.63521 + 200 μg of ALFQ adjuvant	200μg ALFQ	Arm 1: An injection containing 300 μg A244 plus 300 μg B.63521 with 200 μg of ALFQ adjuvant will be administered as an IM injection into the deltoid muscle at visits 1, 3, and 5 (corresponding to Day 1, Day 29, and Day 57).
A244/B.63521 + 100 μg of ALFQ adjuvant	A244	Arm 2: An injection containing 300 μg A244 plus 300 μg B.63521 with 100 μg of ALFQ adjuvant will be administered as an IM injection into the deltoid muscle at visits 1, 3, and 5 (corresponding to Day 1, Day 29, and Day 57).
A244/B.63521 + 50 μg of ALFQ adjuvant	A244	Arm 3: An injection containing 300 μg of A244 plus 300 μg B.63521 with 50 μg of ALFQ adjuvant will be administered as an IM injection into the deltoid muscle at visits 1, 3, and 5 (corresponding to Day 1, Day 29, and Day 57).
A244/B.63521 + 200 μg of ALFQ adjuvant	A244	Arm 1: An injection containing 300 μg A244 plus 300 μg B.63521 with 200 μg of ALFQ adjuvant will be administered as an IM injection into the deltoid muscle at visits 1, 3, and 5 (corresponding to Day 1, Day 29, and Day 57).
A244/B.63521 + 50 μg of ALFQ adjuvant	B.63521	Arm 3: An injection containing 300 μg of A244 plus 300 μg B.63521 with 50 μg of ALFQ adjuvant will be administered as an IM injection into the deltoid muscle at visits 1, 3, and 5 (corresponding to Day 1, Day 29, and Day 57).
A244/B.63521 + 100 μg of ALFQ adjuvant	B.63521	Arm 2: An injection containing 300 μg A244 plus 300 μg B.63521 with 100 μg of ALFQ adjuvant will be administered as an IM injection into the deltoid muscle at visits 1, 3, and 5 (corresponding to Day 1, Day 29, and Day 57).
A244/B.63521 + 100 μg of ALFQ adjuvant	100μg ALFQ	Arm 2: An injection containing 300 μg A244 plus 300 μg B.63521 with 100 μg of ALFQ adjuvant will be administered as an IM injection into the deltoid muscle at visits 1, 3, and 5 (corresponding to Day 1, Day 29, and Day 57).
A244/B.63521 + 50 μg of ALFQ adjuvant	50μg ALFQ	Arm 3: An injection containing 300 μg of A244 plus 300 μg B.63521 with 50 μg of ALFQ adjuvant will be administered as an IM injection into the deltoid muscle at visits 1, 3, and 5 (corresponding to Day 1, Day 29, and Day 57).

Primary Outcome Measures

Name	Time	Method
Incidence of Adverse Events (AEs), Serious Adverse Events (SAE), Adverse Events of Special Interest (AESI), and unsolicited AEs	Days 0 to 393	The number of participants with AEs, SAEs, AESIs, and unsolicited AEs on Day 0 through Day 337 as assessed by the Division of AIDS (DAIDS) grading scale and possible attribution to Investigational Product. The number of participants with medically attended AE will be followed until Day 393.
Number of Participants with Local and Systemic Reactions	Days 0 to 14 post vaccination	Post-vaccination reactions, including redness/erythema, induration, pain/tenderness, itching, warmth, fever, chills, myalgia, arthralgia, headache, nausea, fatigue, rash, and dizziness, will be assessed and recorded on diary cards on Days 0 through 14.

Secondary Outcome Measures

Name	Time	Method
Number of Participants with HIV-specific Binding Antibodies	Day 0 to 336	Vaccine-induced humoral immune responses will be assessed by HIV-specific binding antibody assays, HIV-specific neutralizing antibody assays, and non-neutralizing antibody function assays. HIV-specific cell-mediated responses will be assessed by intracellular cytokine staining, cluster of differentiation 4 (CD4) and cluster of differentiation 8 (CD8) T cell proliferation, and related assays. Innate immune responses and genetic responses will be assessed with flow cytometric panels, DNA microarrays, and RNA sequencing. Blood draws to complete assessments will be obtained at each study visit.

Trial Locations

Locations (1)

Walter Reed Army Institute of Research, Clinical Trials Center; 🇺🇸 Silver Spring, Maryland, United States