IX-01 Effect on Intravaginal Ejaculatory Latency Time (IELT), Patient Reported Outcomes and Safety in Men With Premature Ejaculation (PE)

Inclusion Criteria:

1. Men aged ≥18 years and ≤60 years in stable (≥6 months) heterosexual relationship and
who have lifelong PE.

2. Premature ejaculation ≤1 minute on ≥75% attempts at sexual intercourse during the
run-in period.

3. Meets other aspects of ISSM definition.

4. Patient and partner willing to attempt intercourse at least 4 times during the run-in
period and at least 8 additional times during the double-blind part of the study.

5. Partner not planning pregnancy and willing to use contraception (unless not of
childbearing potential, e.g, surgically sterilized).

6. Willing to limit use of alcohol on days in which he takes study drug.

7. Capable of giving written informed consent.

Exclusion Criteria:

1. IELT value >2 minutes during the run-in period.

2. <4 attempts at sexual intercourse during the run-in period.

3. Any patient who rates his control of ejaculation as fair, good, or very good.

4. Any patient who rates his ejaculation-related "personal distress" as "not at all" or
"a little bit".

5. Erectile Dysfunction.

6. Concomitant use of phosphodiesterase type 5 (PDE5) inhibitors, selective serotonin
reuptake inhibitor (SSRIs)/selective serotonin norepinephrine reuptake inhibitor
(SSNRIs), monoamine oxidase inhibitors, alpha blockers, 5-alpha reductase inhibitors,
topical anesthetics, and/or tramadol.

7. History (last 6 months) of use of Botox or similar product to treat PE.

8. Has received IX-01 in a previous clinical study.

9. Unwilling to stop other treatments for PE (including but not limited to
pharmacological, sex therapy, psychotherapy multiple condoms, and prior
masturbation).

10. Any other sexual disorder of patient or partner that could interfere with results.

11. Any current sexually transmitted disease.

12. Any major medical condition of patient that could interfere with ability to have
sexual activity and/or require hospital treatment.

13. Body mass index (BMI) >40 kg/m2 or weight <60 kg.

14. Participation in a clinical drug study anytime during the 30 days prior to screening.

15. Human immunodeficiency virus (HIV), hepatitis B.

16. History of prostate disease or clinically significant prostate disease.

17. History of myocardial infarction, coronary bypass surgery, coronary artery
angioplasty, unstable angina, clinically evident congestive heart failure, cardiac
pacemaker, or cerebrovascular accident.

18. Known or suspected history of significant cardiac arrhythmias.

19. History of drug-induced allergic reactions including skin reactions.

20. Significant psychiatric disease and/or risk of suicidal tendency.

21. History of or other evidence of recent alcohol or drug abuse.