Inclusion Criteria:
1. Male and female patients aged ≥ 18 years and weighing ≥ 40 kg, able to understand and consent in English, who have been fully informed and:
a) who have given voluntary written informed consent, or whose legally authorized representative(s) has been fully informed and has given voluntary written informed consent if applicable, and in compliance with local regulations OR
2. b) who have given oral informed consent witnessed in writing by an independent person and in compliance with local regulations for patients who are unable to write and/or read but who fully understand the oral information given by the Investigator (or nominated representative).
3. Ongoing coccidioidomycotic meningitis diagnosed within 8 weeks prior to enrolment.
4. Ongoing symptoms due to coccidioidomycosis are such that the risk-benefit of treatment with an investigational agent with a hepatic signal requiring careful monitoring is judged favorable based on meeting criteria
5. Female patients must be non-lactating and at no risk of pregnancy for one of the following reasons:
- Postmenopausal for at least 1 year;
- Post-hysterectomy and/or post-bilateral oophorectomy;
- Of childbearing potential, with a negative urine or serum human chorionic gonadotropin pregnancy test at the screening visit and must be using one of listed below highly effective method of birth control throughout the course of the study period and up to and including 30 days after stopping study drug
- Established use of oral, injected, transdermal, intravaginal, or implanted hormonal methods of contraception associated with inhibition of ovulation
- Placement of an intrauterine device or intrauterine hormone-releasing system
- Male sterilization
- Bilateral tubal occlusion
- Sexual abstinence (reliable sexual abstinence is acceptable but periodic abstinence \[e.g., calendar, ovulation, symptom-thermal, or post-ovulation methods\] and withdrawal are not acceptable).
6. Male patients with female partners of childbearing potential must either totally abstain from sexual intercourse or use a highly effective means of contraception throughout study participation and agree to continue its use for 30 days after stopping study drug and may not donate semen during this time.
Exclusion Criteria:
1. Patients who are unconscious.
2. Patients who are pregnant or breastfeeding.
3. Known history of allergy, hypersensitivity, or any serious reaction to any component of the olorofim.
4. Patients with or planned placement of indwelling CNS hardware (e.g. reservoirs, shunts, ventriculostomies, or external drainage tubes).
5. Patients with a second fungal infection requiring systemic antifungal treatment or prophylaxis, other than Pneumocystis jirovecii infections and cutaneous fungal infections treated topically.
6. Patients with microbiological findings (e.g., bacteriological, virological) or other potential conditions that are temporally related and suggest a different than study indication etiology.
7. HIV infection but not currently receiving antiretroviral therapy. In cases where HIV infection is first diagnosed at the same time as the invasive fungal infection, if antiretroviral therapy is commenced at the time of enrollment, then such patients are eligible for enrolment
8. Any known or suspected medical condition or social circumstance of the patient that may jeopardize adherence to the protocol requirements or impede the accurate measurement of efficacy.
9. Patients with a concomitant medical condition that, in the opinion of the Investigator, may be an unacceptable additional risk to the patient should he/she participate in the study.
10. Patients who have received prior treatment with olorofim/F901318.
11. Treatment with any investigational drug within the 30 days prior to the first administration of study drug except for unblinded protocols (eg, open-label oncological regimen variations or biologic studies). Prior to enrolling patients who are on other open-label studies, it is the site's responsibility to ensure that the study criteria for that study allow for enrollment into this study.
12. Patients receiving treatment limited to supportive care due to predicted short survival time.
13. Patients with a baseline prolongation of QT using Fridericia's Correction Formula (QTcF) ≥ 500 msec, or at high risk for QT/QTc prolongation, eg,
1. A family history of long QT syndrome
2. Other known pro-arrhythmic conditions
3. Risk factors for Torsade de Pointes (e.g., uncompensated heart failure, abnormal plasma potassium or magnesium levels that cannot be corrected, an unstable cardiac condition during the last 30 days).
14. Evidence of hepatic dysfunction with any of the following abnormal laboratory parameters at screening:
1. Total bilirubin ≥ 2 × upper limit of the normal range (ULN), OR
2. Alanine transaminase (ALT) or aspartate transaminase (AST) ≥ 3 × ULN, OR
3. Patients with known cirrhosis or chronic hepatic failure (regardless of ALT/AST/total bilirubin).
Liver transplant recipients may be enrolled if their laboratory parameters do not meet the laboratory exclusions given above.
15. Prohibited concomitant medications. Concomitant administration of inhibitors of human dihydro-orotate dehydrogenase (DHODH), teriflunomide, leflunomide, and systemic use of cannabis/cannabinoid preparations, including tetrahydrocannabinol (THC) and cannabidiol (CBD) are prohibited. There are currently no other absolutely prohibited concomitant medications for olorofim but there are medications with potentially significant drug-drug interactions (DDIs) with olorofim or SOC and the management of potential interactions should be considered before study enrollment.