Phase 1 Randomised, Single-centre, Observer-blind, Placebo-controlled Trial of Safety and Immunogenicity of EN41-UGR7C HIV Vaccine Candidate Administered Intramuscularly in Healthy Female Volunteers

Study start date: April 1, 2013

Inclusion Criteria: Women aged between 18 and 55 years on the day of screening Available for a maximal study duration of 8 months from screening Willing and able to give written informed consent At low risk of HIV infection and willing to remain so for the duration of the study defined as: no history of injecting drug use in the previous ten years no gonorrhoea or syphilis in the last six months no high risk partner (e.g. injecting drug use, HIV infected sexual partner) either currently or within the past six months no unprotected vaginal or anal intercourse in the last six months outside a relationship with a regular partner known to be HIV negative no unprotected sex with someone from a high HIV prevalence region where HIV is more common than in the UK (e.g. Sub-Saharan Africa, Caribbean, South-East Asia) Negative HIV1/2 antibody/antigen test result at screening If heterosexually active female, using an effective method of contraception using a double barrier method of contraception (combined oral contraceptive pill, injectable or implanted contraceptive and use of condoms incorporating spermicide; physiological or anatomical sterility) from 14 days prior to the first vaccine administration until 3 months after the last administration, and willing to undergo urine pregnancy tests prior to each vaccine administration and blood pregnancy test at screening and final follow-up visits. Heterosexual females who become sexually active during the trial should also follow the same guidance Agree to abstain from donating blood during their participation in the trial Registered with a General Practitioner and medical history available for 12 months before dosing Satisfactory response received from General Practitioner relating to medical history before randomization Exclusion Criteria: Pregnant or lactating or planning to get pregnant within the next year Clinically relevant abnormality on history or examination: central nervous system disorder or disease, including history of grand-mal epilepsy severe eczema clinically significant haematological, cardio-pulmonary, metabolic, gastrointestinal, renal, psychiatric or ophthalmological disorders acute infection or illness autoimmune disease, immunodeficiency or use of immunosuppressive agents in preceding 3 months prior to dosing Known hypersensitivity to any component of the vaccine formulation used in this trial, or have severe or multiple allergies History of severe local or general reaction to previous vaccination defined as: local: extensive, indurated redness and swelling involving most of the antero-lateral thigh or the major circumference of the arm, not resolving within 72 hours general: fever >39.5°C within 48 hours; anaphylaxis; bronchospasm; laryngeal oedema; collapse; convulsions or encephalopathy within 72 hours Receipt of live attenuated vaccine within 60 days or other vaccine within 14 days of schedules study vaccine dosing Receipt of an experimental vaccine containing HIV envelope proteins at any time in the past Receipt of blood products or immunoglobulin within 4 months of screening Participation in another trial of a medicinal product, completed less than 90 days prior to Visit 2 and planned participation in another clinical trial during the present trial HIV 1/2 antibody/antigen positive or indeterminate on screening Positive for hepatitis B surface antigen, hepatitis C antibody or serology indicating active syphilis requiring treatment Clinically significant abnormal result in routine laboratory parameters. Unable to read and speak English to a fluency level adequate for the full comprehension of study and procedures required in participation and consent Unlikely to comply with protocol History of drug or alcohol abuse or regular use of drugs, or who test positive for alcohol test at screening On regular medication which in the opinion of the investigator makes volunteer unsuitable for participation in the study Any local vaginal, cervical or gynaecological condition which may interfere with collection or interpretation of data collected through vaginal samples Using any Intra Uterine Contraceptive Device as there is a risk of dislodging, displacing or removing the device when pulling or removing Softcup used for vaginal sampling Clinically significant abnormality on ECG performed at the screening visit Any condition that, in the investigator's opinion, compromises the volunteer's ability to meet protocol requirements or to complete the study