A Phase 1 Trial for Evaluation of the Safety, Pharmacokinetics, and [18F] Radiation Dosimetry of CTT1057

The sponsor has developed a PET imaging agent, CTT1057, labeled with 18F, that is based on a
small molecule core and targets an extracellular region of PSMA with high affinity. Although
comparable to other inhibitors in terms of affinity for PSMA, this unique class of
phosphoramidate agents are the only known irreversible PSMA inhibitors. Due to its
irreversible binding to PSMA and rapid uptake by PSMA-expressing prostate cancer cells,
accumulation at the cancer target is expected to be rapid, specific and sensitive.

Twenty patients will be enrolled in parallel in two cohorts:

- (Cohort A) Patients with prostate cancer prior to radical prostatectomy (N = 5).

- (Cohort B) Patients with evidence of metastatic castration-resistant prostate cancer (N
= 15)

Participants receive a single intravenous (IV) dose (370 MBq, or 10 mCi) of CTT1057 in this
first-in-human trial. Combined PET/MR imaging (prostate + whole body) will be performed
following tracer injection. The 5 patients in the pre-prostatectomy cohort will comprise the
dosimetry/pharmacokinetic (PK) cohort to establish organ dosimetry and PK profile. Patients
in cohort A will undergo planned radical prostatectomy (plus lymph node dissection) within 12
weeks following CTT1057 PET/MR. Patients in cohort B (metastatic prostate cancer) will have
the option for metastatic tumor biopsy following CTT1057 PET imaging.

The one-time nominal injected dose will be 370 MBq (10 mCi). Estimated mass dose is 20 µg of
CTT1057. Dose will be in a volume of 3 - 5 mL, and will be injected intravenously as a bolus
injection.

Vital signs, adverse event assessment, and 12 lead ECGs will be performed on day 1 before and
after dosing.

Inclusion Criteria:

- Male patients age ≥18 years old

- Histologically confirmed adenocarcinoma of the prostate

- Adequate organ function including:

- - Platelet count of > 50,000/mm3

- - Neutrophil count of > 1000/mm3

- - Serum Cr < 1.5 x ULN or estimated GFR > 60 ml/min based upon Cockroft-Gault equation

- - Proteinuria < 1 g/24 hours based upon 24 hour urine collection or spot urine
protein/creatinine ratio

- - AST and ALT < 2.5 x ULN (< 5 x ULN in patients with known liver metastases)

- - Total bilirubin < 1.5 x ULN (< 3 x ULN in patients with known/suspected Gilbert's
disease)

- ECOG performance status of 0 or 1

- Able to provide written informed consent and willing to comply with protocol
requirements

- No contra-indication to MR including severe claustrophobia, incompatible aneurysm
clips or cardiac pacemaker

- For men of childbearing potential, the use of effective contraceptive methods during
the trial and within 6 months following radiotracer injection

- Cohort A only (N = 5 evaluable patients):- Planned radical prostatectomy within 12
weeks following protocol scan

- - No androgen deprivation, anti-androgen therapy, chemotherapy, or investigational
systemic therapy prior to CTT1057 PET imaging

- Cohort B only:- Presence of at least three distinct metastatic lesions by standard
imaging including whole body bone scan + cross-sectional imaging of the abdomen and
pelvis obtained within 12 weeks prior to protocol scan

- - Castration-resistant disease as defined by PCWG2 criteria

- - Must remain on androgen deprivation therapy for duration of trial if no prior
bilateral orchiectomy

Exclusion Criteria:

- Inadequate venous access per assessment of treating health care provider

- Receipt of radioisotope within 5 physical half lives prior to trial enrollment

- Prior treatment with alpha radiation therapy (Radium Ra 223 chloride; Xofigo™) during
the previous 60 days

- Have a medical condition or other circumstances that, in the opinion of the
investigator would significantly decrease the chances of obtaining reliable data,
achieving the study objectives, or completing the trial.

- Histologic evidence of small cell prostate cancer or neuroendocrine differentiation in
> 50% of biopsy tissue