First-in-human Study of 10-1074-LS Alone and in Combination With 3BNC117-LS

Human Immunodeficiency Virus Clinical Trial

Official title:

A Phase 1, Dose Escalation, First-in-human Study of the Safety and Pharmacokinetics of the Subcutaneous and Intravenous Administration of 10-1074-LS Alone and in Combination With 3BNC117-LS in HIV-infected and HIV-uninfected Individuals

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03554408
• Other study ID #: YCO-0971
• Status: Completed
• Phase: Phase 1
• Start date: June 20, 2018
• Est. completion date: February 4, 2021

Study information

• Verified date: August 2021
• Source: Rockefeller University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This first clinical study of 10-1074-LS will evaluate its safety, tolerability and pharmacokinetics profile when administered alone or in combination with 3BNC117-LS to HIV (human immunodeficiency virus) -infected and HIV-uninfected individuals.

Description:

The proposed study is a Phase 1, dose escalation cohort study of 10-1074-LS alone or in combination with 3BNC117-LS, administered intravenously and subcutaneously in HIV uninfected and HIV-1 infected individuals. Study participants will be administered a single intravenous infusion of 10-1074-LS at 3, 10 or 30 mg/kg, single infusions of the combination of 10-1074-LS and 3BNC117-LS, each dosed at 30 mg/kg, or subcutaneous injections of 10-1074-LS alone or in combination with 3BNC117-LS, and three subcutaneous injections of 10-1074-LS in combination with 3BNC117-LS at three dose ratios. The first four groups administered subcutaneous injections of the product(s) will be randomized, double-blinded, and placebo-controlled to assess potential differences in safety and tolerability of the antibody formulation versus the formulation buffer alone. In the dose ratio portion of the study, participants will be randomized into one of three groups, but the products will be administered in an open-label manner. Groups administered intravenous infusions will be enrolled in an open-label manner. PART A Group 1A (n=8) - HIV-uninfected individuals will be administered one 1 mL (approximately 150 mg) subcutaneous injection of 10-1074-LS or placebo (formulation buffer), in a 3:1 ratio. Group 1B (n=8) - HIV-uninfected individuals will be administered one 2 mL (approximately 300 mg) subcutaneous injection of 10-1074-LS or placebo (formulation buffer), in a 3:1 ratio. Group 2A (n=3) - HIV-uninfected individuals will be administered one intravenous infusion of 10-1074-LS dosed at 3 mg/kg. Group 2B (n=3) - HIV-uninfected individuals will be administered one intravenous infusion of 10-1074-LS dosed at 10 mg/kg. Group 2C (n=3) - HIV-uninfected individuals will be administered one intravenous infusion of 10-1074-LS dosed at 30 mg/kg. Group 3B (n=3) - HIV-infected individuals (on ART) will be administered one intravenous infusion of 10-1074-LS dosed at 10 mg/kg. Group 3C (n=3) - HIV-infected individuals (on ART) will be administered one intravenous infusion of 10-1074-LS dosed at 30 mg/kg. PART B Part B will begin after the Safety Monitoring Committee (SMC) evaluates available safety data from Part A, as detailed below. The SMC will also review available safety data with 3BNC117-LS administered intravenously collected under protocol YCO-0946 prior to enrollment in Part B of this study. The SMC will also review subcutaneous dosing at approximately 150 mg (1 mL) and 300 mg (2 mL), collected under IND 131873 when available and prior to enrollment in Part B of this study. Group 4A (n=8) - HIV-uninfected individuals will be administered one 2 mL (approximately 150 mg of each mAb) subcutaneous injection of 10-1074-LS admixed with 3BNC117-LS or placebo (formulation buffer), in a 3:1 ratio. Group 4B (n=8) - HIV-uninfected individuals will be administered two 2 mL (approximately 300 mg of each mAb) subcutaneous injections of 10-1074-LS admixed with 3BNC117-LS or placebo (formulation buffer), in a 3:1 ratio. Group 5 (n=5) - HIV-uninfected individuals will be administered one intravenous infusion of 10-1074-LS and one intravenous infusion of 3BNC117-LS, each dosed at 30 mg/kg. Group 6 (n=5) - HIV-infected individuals (on ART) will be administered one intravenous infusion of 10-1074-LS and one intravenous infusion of 3BNC117-LS, each dosed at 30 mg/kg. Group 7 (n=6) HIV-uninfected individuals will be administered three subcutaneous injections of 10-1074-LS (100 mg) admixed with 3BNC117-LS (200 mg) (2 mL). Group 8 (n=6) HIV-uninfected individuals will be administered three subcutaneous injections of 10-1074-LS (75 mg) admixed with 3BNC117-LS (225 mg) (2 mL). Group 9 (n=6) HIV-uninfected individuals will be administered three subcutaneous injections of 10-1074-LS (60 mg) admixed with 3BNC117-LS (240 mg) (2 mL). Following mAb or placebo administration, study participants will return for safety assessments on days 1 and 3, and weeks 1, 2 and 4 following each dose, then bi-monthly or monthly until the end of study follow up. All participants will be followed for 48 weeks after last mAb or placebo administration. Serum samples for PK measurements will be collected before and at the end each mAb or placebo administration and at multiple subsequent time points during study follow up. Samples will also be collected for measurement of HIV-1 plasma RNA levels before 10-1074-LS and 3BNC117-LS infusions and at follow up visits according to protocol.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 77
• Est. completion date: February 4, 2021
• Est. primary completion date: February 4, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

Groups 1A-1B, 2A-2C, 4A-4B, 5, 7, 8, 9 (HIV-uninfected):

• Males and females, age 18 to 65
• Amenable to HIV risk reduction counseling and agrees to maintain behavior consistent with low risk of HIV exposure.
• If sexually active male or female, and participating in sexual activity that could lead to pregnancy, agrees to use two effective methods of contraception (i.e. condom with spermicide, diaphragm with spermicide, hormone-eluting IUD, hormone-based contraceptive with condom) from 10 days prior to and nine months after 10-1074-LS and/or 3BNC117-LS administration.
• Female study participants of reproductive potential are defined as pre-menopausal women who have not had a sterilization procedure (e.g. hysterectomy, bilateral oophorectomy, tubal ligation or salpingectomy). Women are considered menopausal if they have not had a menses for at least 12 months and have a FSH of greater than 40 IU/L or if FSH testing is not available, they have had amenorrhea for 24 consecutive months.

Groups 3B-3C, 6 (HIV-infected):

• Males and females, age 18 to 65.
• Confirmed HIV-1 infection.
• HIV-infected individuals on ART with HIV-1 plasma RNA levels < 50 copies/mL.
• Current CD4+ T cell count > 300 cells/µl.
• If sexually active male or female, and participating in sexual activity that could lead to pregnancy or transmission of HIV, agrees to use two effective methods of contraception (i.e. condom with spermicide, diaphragm with spermicide, hormone-eluting IUD, hormone-based contraceptive with condom) from 10 days prior to and nine months after 10-1074-LS and/or 3BNC117-LS administration. Exclusion Criteria:

Groups 1A-1B, 2A-2C, 4A-4B, 5, 7, 8, 9 (HIV-uninfected):

• Confirmed HIV-1 or HIV-2 infection.
• Weight > 110 kg (subcutaneous groups only: 1A-1B, 4A-4B).
• History of immunodeficiency or autoimmune disease; use of systemic corticosteroids, immunosuppressive anti-cancer, or other medications considered significant
• Any clinically significant acute or chronic medical condition (such as autoimmune diseases) that in the opinion of the investigator would preclude participation.
• Within the 12 months prior to enrollment, the participant has a history of sexually transmitted infection.
• Hepatitis B or C infection as indicated by the presence of Hepatitis B surface antigen (HBsAg) or hepatitis C virus RNA (HCV-RNA) in blood.
• Laboratory abnormalities in the parameters listed:
• Absolute neutrophil count = 1,500 cells/µL;
• Hemoglobin = 11 gm/dL if female; = 12.5 gm/dL if male;
• Platelet count = 125,000 cells/µL;
• ALT = 1.25 x ULN;
• AST = 1.25 x ULN;
• Alkaline phosphatase = 1.5 x ULN;by the trial physician within the last 6 months.
• Pregnancy or lactation.
• Any vaccination within 14 days prior to mAb infusions.
• Receipt of any experimental HIV vaccine or monoclonal antibody therapy of any kind in the past.
• History of severe reaction to a vaccine or drug infusion or history of severe allergic reactions.
• Individuals with known hypersensitivity to any constituent of the investigational products.
• Receipt of another investigational product currently or within the past 12 weeks, or expected concurrent participation in another study in which investigational products will be administered.

Groups 3B-3C, 6 (HIV-infected):

• Have a history of AIDS-defining illness within 3 years prior to enrollment.
• History of systemic corticosteroids, immunosuppressive anti-cancer, or other medications considered significant by the trial physician within the last 6 months.
• Any clinically significant acute or chronic medical condition (such as autoimmune diseases), other than HIV infection, that in the opinion of the investigator would preclude participation.
• Hepatitis B or C infection as indicated by the presence of Hepatitis B surface antigen (HBsAg) or hepatitis C virus RNA (HCV-RNA) in blood.
• Laboratory abnormalities in the parameters listed below:
• Absolute neutrophil count = 1,000 cells/µl;
• Hemoglobin = 10 gm/dL;
• Platelet count = 100,000 cells/µl;
• ALT = 1.5 x ULN;
• AST = 1.5 x ULN;
• Alkaline phosphatase = 1.5 x ULN;
• Total bilirubin > 1 x ULN;
• eGFR < 60 mL/min/1.73m2.
• Pregnancy or lactation.
• Any vaccination within 14 days prior to MAb infusions.
• Receipt of any experimental HIV vaccine or monoclonal antibody therapy of any kind in the past.
• History of severe reaction to a vaccine or drug infusion or history of severe allergic reactions.
• Individuals with known hypersensitivity to any constituent of the investigational products.
• Receipt of another investigational product currently or within the past 12 weeks, or expected concurrent participation in another study in which investigational products will be administered.

Related Conditions & MeSH terms

• Acquired Immunodeficiency Syndrome
• HIV Infections
• Human Immunodeficiency Virus

Intervention

Drug:
• 10-1074-LS
Subcutaneous injection of 10-1074-LS
• 10-1074-LS
Intravenous infusion of 10-1074-LS
• 3BNC117-LS
Subcutaneous injection of 3BNC117-LS
• 3BNC117-LS
Intravenous infusion of 3BNC117-LS

Locations

Country	Name	City	State
United States	The Rockefeller University	New York	New York

Sponsors (1)

Lead Sponsor	Collaborator
Rockefeller University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The number of participants who experience adverse events within 2 weeks after 10-1074-LS intravenous infusions and subcutaneous injections.	Adverse events include signs, symptoms and laboratory abnormalities, in addition to local and systemic reactogenicity adverse events.	2 weeks
Primary	The number of participants who experience adverse events within 2 weeks after 10-1074-LS and 3BNC117-LS intravenous infusions and subcutaneous injections.	Adverse events include signs, symptoms and laboratory abnormalities, in addition to local and systemic reactogenicity adverse events.	2 weeks
Primary	Elimination half-life (t1/2) of 10-1074-LS, when administered alone and in combination with 3BNC117-LS in all study groups.	Elimination half-life (t1/2) of 10-1074-LS, when administered alone and in combination with 3BNC117-LS in all study groups.	48-72 weeks
Primary	The clearance (CL) of 10-1074-LS, when administered alone and in combination with 3BNC117-LS in all study groups.	The clearance (CL) of 10-1074-LS, when administered alone and in combination with 3BNC117-LS in all study groups.	48-72 weeks
Primary	The volume of distribution (Vz) of 10-1074-LS, when administered alone and in combination with 3BNC117-LS in all study groups	The volume of distribution (Vz) of 10-1074-LS, when administered alone and in combination with 3BNC117-LS in all study groups	48-72 weeks
Primary	Area under the curve of 10-1074-LS, when administered alone and in combination with 3BNC117-LS in all study groups.	Area under the curve of 10-1074-LS, when administered alone and in combination with 3BNC117-LS in all study groups.	48-72 weeks
Primary	Decay curve of 10-1074-LS, when administered alone and in combination with 3BNC117-LS in all study groups.	Decay curve of 10-1074-LS, when administered alone and in combination with 3BNC117-LS in all study groups.	48-72 weeks
Secondary	Frequency of induced anti-10-1074-LS antibodies	Frequency of induced anti-10-1074-LS antibodies	48-72 weeks
Secondary	Level of induced anti-10-1074-LS antibodies	Level of induced anti-10-1074-LS antibodies	48-72 weeks
Secondary	Frequency of induced anti-3BNC117-LS antibodies	Frequency of induced anti-3BNC117-LS antibodies	48-72 weeks
Secondary	Level of induced anti-3BNC117-LS antibodies	Level of induced anti-3BNC117-LS antibodies	48-72 weeks
Secondary	The number of participants that experience who experience adverse events during the study follow up period after 10-1074-LS and/or 3BNC117-LS administration in all study groups.	Adverse events include signs, symptoms and laboratory abnormalities	48-72 weeks