GS-0415
DrugAdministered SC or IV
NCT Number: NCT07719491
The goals of this clinical study are to learn more about the study drug GS-0415, safety, tolerability, and pharmacokinetics (PK) of single ascending doses (SAD) and multiple ascending doses (MAD) of subcutaneous (SC) and intravenous (IV) GS-0415 in people with HIV-1 (PWH) on antiretroviral treatment.
The primary objectives of this study are to evaluate the safety and tolerability of escalating, single and multiple subcutaneous (SC) and intravenous (IV) doses of GS-0415, administered in PWH who are virologically suppressed on antiretroviral therapy (ART) and to evaluate the pharmacokinetics (PK) of GS-0415.
Trial opening soon.
Get Notified18 year–65 year
All sexes
Interventional
Phase 1
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Key Exclusion Criteria:
1.) Positive anti-HCV antibody and negative HCV polymerase chain reaction (PCR) results are acceptable
2.) Significant serious skin disease, such as but not limited to rash, food allergy, eczema, psoriasis, or urticaria
3.) Significant drug sensitivity or drug allergy ('but not limited to anaphylaxis or drug-induced liver injury)
4.) Known hypersensitivity to the study drugs, their metabolites, or to formulation excipients
5.) Previous or current history of bleeding disorder, platelet disorder including unexplained acute or chronic thrombocytopenia
6.) Autoimmune diseases including Type 1 diabetes mellitus
7.) Serious or active medical or psychiatric illness that would interfere with participant treatment, assessment, or compliance with the protocol.
Note: Other protocol defined Inclusion/Exclusion criteria may apply.
Administered SC or IV
Administered SC or IV
Time frame: First dose date up to 99 days
Time frame: First dose date up to 99 days
Time frame: Up to 43 days
AUCinf is defined as the area under the concentration versus time curve extrapolated to infinite time, calculated as AUClast + (Clast/λz).
Time frame: Up to 43 days
Cmax is defined as the maximum observed concentration of drug.
Time frame: Up to 99 days
AUCtau is defined as the area under the concentration versus time curve over the dosing interval.
Time frame: Up to 99 days
Time frame: Up to 99 days
Time frame: Up to 99 days
Contact information is provided by the study sponsor or research team.
Gilead Sciences
Industry
A First-in-Human Phase 1b, Single-Blind, Placebo-controlled Single Ascending Dose (SAD) and Multiple Ascending Dose (MAD) Study to Evaluate Safety and Pharmacokinetics of GS-0415 in People With HIV-1 Who Are Virologically Suppressed on Antiretroviral Treatment
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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