FAETH Eligibility Criteria

Inclusion Criteria:

Able to provide written informed consent.
Age ≥18 at Visit -1 (screening).
Histologically or cytologically confirmed recurrent solid tumors.
1. Cohort 1a: any extracranial solid tumor
2. Cohort 1b: either recurrent or persistent endometrial adenocarcinoma (EC) with the following histologic epithelial cell types: endometrioid adenocarcinoma, serous adenocarcinoma, undifferentiated carcinoma, clear cell adenocarcinoma, mixed epithelial carcinoma, adenocarcinoma not otherwise specified (N.O.S.), mucinous adenocarcinoma, squamous cell carcinoma, transitional cell carcinoma, and carcinosarcoma or; ovarian cancer (OC) with the primary tumor having ≥ 50% clear cell histomorphology or ovarian clear cell or ovarian endometrioid carcinoma.
3. Cohort 2: adenocarcinoma of the colon or rectum.
4. Cohort 3: recurrent or persistent endometrial adenocarcinoma with the following histologic epithelial cell types as described for Cohort 1b
5. Cohort 4: OC primary tumor carcinomas as described for Cohort 1b
Tumor must harbor an activating mutation in the PIK3CA gene with or without PTEN loss, either previously documented or determined during screening.
Fresh or archival tumor biopsy with sufficient material to be sent to the designated laboratory for PD analyses. For patients who consent to future research, an additional 5 slides from a surgical specimen or biopsy is required.
Cohort 1a - Dose Modification (subjects with any solid tumor): failed, were intolerant of, or ineligible for no more than 3 prior lines of therapy (LOT) for advanced/metastatic disease or refused SOC therapy.
For all cohorts, in the unlikely scenario that a subject refused all available SOC they may proceed with trial. These subjects would be regarded as having 0 prior LOT.
Cohorts 1b, 2, 3, and 4 - failed, were intolerant of, ineligible for, or have refused SOC therapy for advanced/metastatic disease (AJCC stage III and IV) and:
1. Cohort 2 (subjects with colorectal cancer): Have failed no more than 2 prior LOT for metastatic CRC.
2. Cohort 1b, Cohort 3 (subjects with endometrial cancer): Have no more than 3 prior chemotherapeutic regimens for management of endometrial carcinoma (neo-adjuvant and/or adjuvant chemotherapy will be counted as 1 prior LOT). Prior hormonal therapy will not count as a systemic regimen.
3. Cohort 1b, Cohort 4 (subjects with clear cell or endometrioid OC): Subjects must have had no more than 3 prior chemotherapeutic regimens for management of ovarian carcinoma. Prior hormonal therapy will not count as a systemic regimen.
Life expectancy of at least 3 months.
At least one measurable lesion (as defined by Response Evaluation Criteria in Solid Tumors [RECIST] 1.1).
ECOG PS of 0 to 1.
Adequate organ function
1. Absolute neutrophil count (ANC) ≥1.0 × 10^9/L, platelet count ≥75 × 10^9/L, and hemoglobin ≥8.5 gm/dL (may be transfused to reach this hemoglobin level unless due to blood loss).
2. Liver transaminases (AST and ALT) ≤2.5 × upper limit of normal (ULN) (<5 × ULN if liver metastases are present), and total bilirubin ≤1.5 × ULN (<3 x ULN if subject has Gilbert Syndrome).
3. INR ≤1.5 x ULN unless subject is on anticoagulants that would affect the INR, then INR must be in the desired therapeutic range as judged by the Investigator.
4. Albumin level ≥3.0 mg/dL or ≥ the lower limit of normal.
5. Renal: Serum creatinine ≤2 x ULN
Ability to take oral medication, be willing to adhere to study procedures and Study Drug administration, and receive, consume, and comply with Study ISD.
For women of child-bearing potential, a negative serum pregnancy test collected at screening (V-1) and negative urine pregnancy test collected at baseline (V0) and use of physician-approved method of birth control from the time of the pregnancy test performed at screening to 90 days following the last administration of Study Drug or, if applicable, 6 months following the last administration of nab-paclitaxel.
Male subjects must be surgically sterile or must agree to use physician-approved contraception during the study and for 90 days following the last administration of Study Drug.

Exclusion Criteria:

Diagnosis of primary brain tumor.
Has had serabelisib, alpelisib, or other PI3K inhibitor.
Leptomeningeal disease and symptomatic or untreated brain metastases.
Diagnosis of, or requiring treatment for, another malignancy within the past 2 years (excluding a history of carcinoma in situ of the cervix, superficial non-melanoma skin cancer, or superficial bladder cancer that has been adequately treated, or stage 1 prostate cancer that does not require treatment or requires only treatment with luteinizing hormone-releasing hormone agonists or antagonists if initiated at least 90 days prior to the first dose of Study Drug).
Is less than 21 days from therapeutic radiation or chemotherapy prior to the first day of dosing with Study Drug and has not recovered to Grade ≤ 1 from all clinically significant toxicities related to prior therapies.
For subjects receiving nitrosoureas or mitomycin C, the subject is < 6 weeks from last dose. For monoclonal antibody therapy, the subject is < one half-life or <4 weeks from the last dose.
Chronic, systemically administered glucocorticoids in doses equivalent to >5 mg prednisone daily. Replacement corticosteroids for adrenal insufficiency are permitted.
Diabetes mellitus requiring insulin or insulin secretagogue therapy.
Poorly controlled diabetes mellitus defined as glycosylated hemoglobin A1c (HbA1c) >7.5% or fasting blood sugar >160 mg/ dL.
Known impaired cardiac function or clinically significant cardiac disease.
QTcF interval >470 msec found at screening.
Myocardial infarction, cardiac stent placement, or unstable angina within 6 months before the first administration of Study Drug.
Have clinically significant peripheral vascular disease.
Manifestations of malabsorption
Other clinically significant comorbidities.
Pregnant (positive serum pregnancy test), planning to become pregnant during the study, or breastfeeding/planning to breastfeed during the study.
Have taken strong CYP3A4 inducers/inhibitors within 7 days before the first administration of serabelisib or have conditions that require the concomitant use of CYP3A4 inducers/inhibitors.
Untreated or poorly controlled, gastro-esophageal reflux disease.
Have taken histamine-H2 receptor antagonists within 24 hours before the first administration of serabelisib.
Have taken PPI within 7 days or 5 half-lives (whichever is the shorter duration) before the first administration of serabelisib or are anticipated to need PPI during the study.
Have taken neutralizing antacids within 4 hours before the first administration of serabelisib or are anticipated to need frequent antacid use during the study.
Subjects with poorly controlled human immunodeficiency virus (HIV), hepatitis B virus (HBV), and/or hepatitis C virus (HCV) infections.
Known allergies to serabelisib excipients or the ISD
Severe, uncontrolled gout.
A BMI <18.5 kg/m2, or serious or refractive cachexia or anorexia that, in the Investigator's opinion, realistically prohibits subjects from having energy or appetite sufficient to reliably engage in a strict medical food regimen for an extended time.
Any condition that renders the subject unable to satisfactorily chew, swallow, digest, or tolerate (i.e., persistent diarrhea) the majority of foods and liquids of the Study ISD.
History of severe nephrolithiasis requiring urologic intervention.
Participation in a diet or weight loss plan within 10 days prior to the first administration of Study Drug.
Severe constipation or condition where exacerbation of constipation is not advisable (eg, small bowel obstruction history).
History of anaphylaxis from food allergy or other disease state requiring avoidance of a particular food, such as celiac disease.
Diagnosed eating disorder in the past 10 years.
Unwilling to take a non-vegan or non-vegetarian diet.
Peripheral neuropathy ≥ CTC Grade 2