Trial of a Falciparum Malaria Protein (FMP012), E. Coli-expressed PfCelTOS, in Healthy Malaria-Naive Adults

Single center, non-randomized, open label, dose escalation Phase 1study with sporozoite
challenge. The antigen FMP012 will be adjuvanted with Glucopyranosyl lipd A stable emulsion
(GLA-SE), a proprietary adjuvant produced by the Infectious Disease Research Institute
(IDRI). This is a first-in-human study of FMP012. Thirty subjects, divided into 3 groups (10
subjects per group), will receive 3 doses of the FMP012/GLA-SE vaccine. Group 1 will receive
10 µg of FMP012 formulated with 2 µg GLA-SE adjuvant and Group 2 will receive 10 µg of
FMP012 formulated with 5 µg GLA-SE adjuvant. Group 3 will receive 50 µg of FMP012 formulated
with either 5 µg GLA-SE adjuvant (Group 3a) or 2 µg GLA-SE adjuvant (Group 3b).
Determination of whether to proceed with Group 3a or Group 3b will be made by the principal
investigator (PI) and the independent medical monitor after the second vaccination dose in
Group 2 has been completed, based on predefined safety and group hold criteria in this
protocol. There will be a staggered start for Group 1 and Group 2 separated by a minimum of
14 days. Group 3a or Group 3b will start vaccinations 2 weeks after the second vaccination
for Group 2. The first and second vaccination doses in each group will be separated by 28
days and all groups will receive the third vaccination dose on the same day. The second and
third vaccination doses in Group 1 will be separated by 84 days, Group 2 by 70 days, and
Group 3 by 28 days. Six non-immunized infectivity control subjects will be enrolled prior to
the challenge phase. All subjects from the Vaccination Group and Infectivity Control Group
will participate in the primary malaria sporozoite challenge and will be required to stay at
a hotel for evaluation for a maximum of 10 nights starting 9 days after the challenge. A
directly monitored, sequentially allocated, open-label oral regimen of chloroquine or
artemether/lumefantrine will be administered to all parasitemic subjects.

- Healthy adults (male or non-pregnant, non-lactating female) 18 to 50 years of age at
the time of screening

- If the subject is female,

- Non-childbearing potential , abstinent or using adequate contraceptive precautions
during this study and must agree to continue such precautions until three months
after challenge

- A negative pregnancy test at the time of enrollment

- Free of significant health problems as established by medical history, laboratory,
and clinical examination before entering the study

- Low cardiac risk factors

- Available to participate and reachable by phone for duration of study (approximately
8 months)

- No plans to travel to outside the Washington DC area between the day of challenge and
either completion of treatment course (post-challenge) or, if subject remains
uninfected, 28 days post-challenge

- No plans to travel to a malaria endemic area during the course of the study

- Written informed consent must be obtained from the subject before screening
procedures

- Subjects must score at least 80% correct on a multiple-choice quiz that assesses
their understanding of this study

- Active duty military must obtain approval from his or her supervisor

Exclusion Criteria:

- History of malaria infection

- History of travel to P. falciparum endemic areas in the 3 months prior to day of
first vaccination or day of challenge

- History of receiving a malaria vaccine

- Receipt of any licensed vaccine within 7 days prior to first vaccination

- History of receipt of malaria prophylaxis during the 2 months prior to day of first
vaccination or day of challenge

- History of use of any drugs with significant antimalarial activity during the course
of the study period

- Prior receipt of any vaccine containing either QS-21, MPL or GLA-SE in the previous 5
years (including Cervarix®, GSK)

- Use of any investigational or non-registered drug or vaccine within 30 days preceding
the first dose of study vaccine or planned use during the study period.

- Any history of allergic reaction or anaphylaxis to previous vaccination

- Allergy to kanamycin, nickel, or imidazole Pregnant or lactating female at screening
or plans to become pregnant or breastfeed from the time of enrollment until three
months after challenge

- Allergy to antimalarial drugs or use of medications known to interact with both CQ
and artemether/lumefantrine

- Significant (eg, systemic) hypersensitivity reactions to mosquito bites

- History of sickle cell disease

- History of psoriasis or porphyria

- History of splenectomy

- Any confirmed or suspected immunodeficiency, including HIV infection

- Administration of chronic (defined as more than 14 days) immunosuppressive drugs or
other immune-modifying drugs within six months of vaccination

- Inhaled and topical steroids are allowed

- A family history of congenital or hereditary immunodeficiency

- Acute or chronic, clinically significant, pulmonary, cardiovascular, hepatic, or
renal functional abnormality, as determined by history, physical examination, or
laboratory evaluation

- Chronic or active neurologic disease including seizure disorder and chronic migraine
headaches

- Administration of immunoglobulins and/or any blood products within the three months
preceding the first dose of study vaccine or any planned administration during the
study period

- Any abnormal baseline laboratory screening tests listed below (normal values are
defined in the adverse event section of this protocol):

- Seropositive for HIV or Hepatitis C virus or HBsAg positive

- Hepatomegaly, right upper quadrant abdominal pain or tenderness

- An abnormal baseline screening EKG.

- Suspected or known current alcohol or drug abuse as determined from the medical
history or by physical examination

- Any other significant finding that in the opinion of the PI would increase the risk
of having an adverse outcome from participating in this study