Is NCT06310551 recruiting in Salt Lake City, UT?

Yes, NCT06310551 is currently recruiting participants at its Salt Lake City, UT location. This hiv infections clinical trial is actively enrolling qualified participants.

How do I join the hiv infections clinical trial in Salt Lake City?

To join this clinical trial in Salt Lake City, complete the eligibility form on this page. A study coordinator will contact you to discuss next steps and determine if you qualify.

Is participation in this Salt Lake City clinical trial free?

Yes, all study-related care is provided at no cost to qualified participants. Many studies also offer compensation for time and travel expenses.

HIV Infections Clinical Trial in Salt Lake City, UT

Who Can Participate

Inclusion Criteria

Participant must be 18 to 55 years of age inclusive, at the time of signing the informed consent. Type of Participant and Characteristics

Participants who are overtly healthy as determined by medical evaluation including medical history, physical examination, laboratory tests, and cardiac monitoring.

Participants who are negative for SARS-CoV-2, performed on admission/readmission to the Phase 1 unit, using an approved molecular test (PCR).

Participants who are able to understand and comply with protocol requirements and timetables, instructions, and protocol-stated restrictions. Weight

Body weight ≥50.0 kg (110 lbs) for men and ≥45.0 kg (99 lbs) for women and body mass index within the range 18.5 to 32.0 kg/m\^2 (inclusive) for all cohorts except B19. For Cohort B19, body mass index within the range \>32.0 to 37.0 kg/m\^2 (inclusive). Sex and Contraceptive/Barrier Requirements

Male or female

Male Participants: No restrictions for male participants

Participants of female sex assigned at birth:

A participant of childbearing potential (POCBP) (female sex assigned at birth) is eligible to participate as long as the participant is not pregnant, breastfeeding and utilizes a highly effective method of contraception.

A participant of non-childbearing potential (PONCBP) is eligible to participate if all other eligibility criteria are met. Informed Consent

Capable of providing signed informed consent.

Exclusion Criteria

Medical Conditions

History or presence of clinical condition or disorder that could be capable of significantly altering the absorption, metabolism, or elimination of drugs; constituting a risk when taking the study drug, interfering with the interpretation of data or would make the participant unsuitable for the study; unable to comply with dosing requirements; or unable to comply with study visits.

Clinically significant abnormal blood pressure as determined by the investigator.

Lymphoma, leukemia, or any malignancy within the past 5 years except for basal cell or squamous epithelial carcinomas of the skin that have been resected with no evidence of metastatic disease for 3 years.

Breast cancer within the past 10 years.

Current or chronic history of liver disease or known hepatic or biliary abnormalities.

Medical history of cardiac arrhythmias or cardiac disease or a family and personal history of long QT syndrome.

Underlying skin disease or disorder that would interfere with the administration of study product and/or assessment of injection site reactions.

Clinically significant history of drug hypersensitivity, delayed-type hypersensitivity or severe hypersensitivity reactions, as well as history of /sensitivity to any of the study interventions including hyaluronidases.

Current or anticipated need for chronic anti-coagulation except for the use of low dose acetylsalicylic acid (≤325 mg) or hereditary coagulation and platelet disorders such as hemophilia or Von Willebrand Disease.

History of seizure.

Any known or suspected pre-existing psychiatric condition, including depression, anxiety and insomnia/sleep disturbances, at the discretion of the investigator.

Any positive (abnormal) response confirmed by the investigator or clinician (or qualified designee) administered C-SSRS at screening.

Insufficient muscle mass (gluteus medius or thigh) to support IM dose administration in the opinion of the investigator.

Presence of tattoos, implants or skin piercings that may interfere with the administration of study product and/or assessment of ISRs, if they occur.

History of or on-going high-risk behaviors that may put the participant at increased risk for HIV acquisition in the opinion of the investigator. This includes participants in HIV discordant relationships, or men who report current or prior unprotected anal sex with other men and those reporting prior or current injecting drug use. Prior/Concomitant Therapy

Past or intended use of over-the-counter or prescription medication within 7 days (or 14 days if the drug is a potential enzyme inducer) or 5 half-lives (whichever is longer) prior to dosing and for the duration of the study.

Receipt of any live vaccine(s) or vaccines against SARS-CoV-2 within 28 days prior to screening or 14 days before or after scheduled SC or IM dosing. Prior/Concurrent Clinical Study Experience

Exposure to more than 4 new investigational products (including long-acting investigational products) within 12 months prior to the first dosing day.

Current enrollment or past participation in another investigational study in which an investigational intervention was administered within the last 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product before signing of consent (OR screening) any other clinical study.

Participation in the study would result in loss of blood in excess of 500 mL over a 56-day period.

Current enrollment or past participation in this clinical study, with the exception of participants who previously completed the Oral Lead In (OLI) but for operational or logistic reasons did not progress to CRU admission and receipt of injectable suspension for injection (SFI) or powder for suspension for injection (PFS) study medication or placebo, or prior participation in study 218803. Diagnostic Assessments

eGFR \<60 mL/min or serum creatinine \>1.1 x ULN.

Hemoglobin \<12.5 g/dL for men and \<11 g/dL for women

ALT or AST \>1.5x upper limit of normal (ULN)

Total bilirubin \>1.5xULN.

Any significant arrhythmia or ECG finding.

Presence of HBsAg and/or anti-HBc at Screening or within 3 months prior to first dose of study intervention.

Positive hepatitis C antibody test result at screening or within 3 months prior to first dose of study intervention.

Positive pre-study drug/alcohol screen.

Positive HIV antibody test. Other Exclusions

Regular alcohol consumption within 6 months prior to the study defined as: An average weekly intake of \>14 units for males or \>7 units for females. One unit is equivalent to 8 g of alcohol: a half-pint (\~240 mL) of beer, 1 glass (125 mL) of wine or 1 (25 mL) measure of spirits.

Regular use of known drugs of abuse.

Urinary cotinine levels indicative of smoking or history or regular use of tobacco- or nicotine-containing products within 6 months prior to screening and at admission.

Sensitivity to the study drug, or components thereof, or other drug or other allergy that, in the opinion of the investigator or Sponsor Medical Monitor, contraindicates participation in the study.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Salt Lake City?

Yes, this clinical trial (NCT06310551) has an active research site in Salt Lake City, UT that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

HIV Infections Treatment Options in Salt Lake City, UT

If you're searching for hiv infections treatment options in Salt Lake City, UT, this clinical trial (NCT06310551) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Salt Lake City research site is actively enrolling participants for this clinical trial. You'll receive care from experienced hiv infections specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all hiv infections clinical trials near you to find additional studies recruiting in your area.

HIV Infections Clinical Trial in Salt Lake City, UT

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About This HIV Infections Study in Salt Lake City