Safety & Efficacy Study of TPI 287 + Avastin in Adults With Glioblastoma That Progressed Following Prior Avastin Therapy

This multi-center trial is a phase 2, dose-escalation study of the safety, tolerability
(MTD), and efficacy of TPI 287 in combination with bevacizumab in subjects who have GBM that
has progressed following prior radiation and TMZ therapy and that has progressed following
prior bevacizumab therapy.

All subjects will be administered TPI 287 as an intravenous (IV) infusion (target duration of
1 hour) once every 3 weeks (Days 1 and 22 of a 42-day cycle) and bevacizumab as a 30 to 90
minute IV infusion once every 2 weeks (Days 1, 15, and 29 of the 42-day cycle). The
subsequent cycle will start 3 weeks after the last TPI 287 infusion and 2 weeks after the
last bevacizumab infusion, maintaining the once every 3 week and once every 2 week schedule,
respectively.

The dose of TPI 287 will be escalated in sequential dose cohorts of 3 to 6 subjects, while
the dose of bevacizumab remains constant (10 mg/kg). The initial cohort of 3 subjects will be
treated at a TPI 287 dose of 140 mg/m2 (dose level 0). The next dose level will be 160 mg/m2
(dose level 1). Subsequent dose levels will be increased in increments of 10 mg/m2 (i.e.,
dose level 2 = 170 mg/m2, dose level 3 = 180 mg/m2, etc.). If dose de-escalation below the
starting dose level is required, dose levels of 130 and 120 mg/m2 will be used. Twelve (12)
to 18 subjects are planned for enrollment during the dose escalation phase, depending on the
number of subjects that experience dose limiting toxicities (DLTs).

Once the MTD is identified, 6 additional subjects will be enrolled at the MTD (for a total of
12) to better characterize the toxicity profile at this level.

Dose modifications and delays will be required as described in the protocol. Subjects may
continue on treatment unless they meet one or more of the discontinuation criteria outlined
in the protocol. Subjects who are discontinued prior to completing Cycle 1 for any reason
other than toxicity will be replaced.

Adverse events (AEs) and concomitant medications will be monitored throughout the study.
Subjects will be given a diary to record any AEs or concomitant medications taken between
visits. Additional safety evaluations will include physical examination (including neurologic
examination), Karnofsky performance status (KPS), weight (body surface area, BSA), vital
signs, hematology, serum chemistry, and urinalysis.

Efficacy evaluations will include magnetic resonance imaging [MRI, including both pre and
post-gadolinium T1-weighted scans and T2/fluid attenuated inversion recovery (FLAIR) images],
corticosteroid usage, and neurologic status (as measured by neurologic exam and KPS).

Inclusion Criteria:

1. Histologically proven GBM

2. Disease progression following radiation & TMZ

3. 1st progression of GBM on bevacizumab-containing regimen or within 8 weeks of
discontinuing bevacizumab. In either case, must have received a minimum of 8 weeks (4
infusions) of bevacizumab.

4. Baseline MRI must be performed after subject signs informed consent form (ICF), within
17 days of Day 1, & on steroid dosage that has been stable or decreasing for at least
5 days

5. Recent resection of recurrent or progressive tumor allowed as long as at least 4 weeks
have elapsed from date of surgery & subject has recovered from surgery

6. Life expectancy >12 weeks

7. Eighteen years old or older

8. KPS equal to or greater than 70

9. Recovered from toxic effects of prior therapy to < Grade 2 toxicity per National
Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) prior to
Day 1. Minimum duration required between prior therapy & Day 1 is:

1. At least 12 weeks from completion of radiation therapy except if there is
unequivocal evidence for tumor recurrence in which case at least 4 weeks

2. 4 weeks from prior cytotoxic therapy

3. 4 weeks from prior experimental drug

4. 6 weeks from nitrosoureas

5. 3 weeks from procarbazine

6. 1 week for non-cytotoxic agents (e.g., interferon, tamoxifen, & cis-retinoic
acid)

7. 14 days from last dose of bevacizumab

10. Adequate bone marrow function [absolute neutrophil count (ANC) > 1,500/mm3 & platelet
count of > 100,000/mm3], adequate liver function [alanine aminotransferase (ALT) &
aspartate aminotransferase (AST) <3 x upper limit normal (ULN), alkaline phosphatase
<2 x ULN, & total bilirubin <1.5 mg/dL], & adequate renal function (BUN & creatinine
<1.5 x ULN)

11. Minimum hemoglobin of 9 g/dL

12. Males & women of childbearing potential must agree to abstain from sex or use an
adequate method of contraception for duration of study & for 6 months after last dose
of study drug

13. Signed & dated ICF prior to Screening evaluations

Exclusion Criteria:

1. Radiographic evidence of contrast-enhancing tumor crossing midline, leptomeningeal
dissemination, gliomatosis cerebri or infratentorial tumor

2. Evidence or suspicion of disease metastatic to sites remote from supratentorial brain

3. Prior treatment with anti-vascular endothelial growth factor (VEGF) drugs other than
bevacizumab

4. Prior treatment with tyrosine-kinase inhibitors targeting VEGF, platelet-derived
growth factor, fibroblast growth factor, tyrosine kinase with immunoglobulin-like and
epidermal growth factor-like domains 2 (TIE-2), or angiopoietin (or their receptors)

5. Prior treatment with histone deacetylase inhibitors or mammalian target of rapamycin
(mTOR) inhibitors

6. Prior treatment with TPI 287

7. Treatment with Enzyme-Inducing Anti-Epileptic Drugs within 2 weeks prior to Day 1

8. Treatment with drugs or herbal supplements known to be strong inhibitors/inducers of
cytochrome P450 3A4 or 2C8 within 2 weeks prior to Day 1

9. Received more than one course of radiation therapy or more than a total dose of 65 Gy.
May have received radiosurgery as part of initial therapy; however, dose counts
against total dose limit.

10. Prior taxane, vincristine, or other microtubule inhibitor chemotherapies for treatment
of GBM or other malignancy

11. Major surgical procedure, open biopsy, or significant traumatic injury within 28 days
prior to Day 1 or anticipation of need for major surgical procedure during course of
study

12. Core biopsy or other minor surgical procedure, excluding placement of a vascular
access device, within 7 days prior to Day 1

13. Any condition, including the presence of clinically significant laboratory
abnormalities, which places subject at unacceptable risk if he/she were to participate
in study or confounds the ability to interpret data from study, including:

1. Active infection including known AIDS or Hepatitis C or with a fever ≥38.5°C
within 3 days prior to study enrollment

2. Diseases or conditions that obscure toxicity or dangerously alter drug metabolism

3. Serious intercurrent medical illness (e.g., symptomatic congestive heart failure)

14. Any serious medical condition, laboratory abnormality, or psychiatric illness that
would prevent subject from providing informed consent

15. Inadequately controlled hypertension (defined as systolic blood pressure >140 mmHg
and/or diastolic blood pressure > 90 mmHg)

16. Prior history of hypertensive crisis or hypertensive encephalopathy

17. New York Heart Association Grade II or greater congestive heart failure

18. History of myocardial infarction or unstable angina within 6 months prior to Day 1

19. History of stroke or transient ischemic attack within 6 months prior to Day 1

20. Significant vascular disease (e.g., aortic aneurysm, requiring surgical repair or
recent peripheral arterial thrombosis) within 6 months prior to Day 1

21. History of hemoptysis (≥ 1/2 teaspoon of bright red blood per episode) within 1 month
prior to Day 1

22. Evidence of bleeding diathesis or significant coagulopathy (in absence of therapeutic
anticoagulation)

23. Grade 2 or higher peripheral neuropathy per NCI CTCAE

24. History of abdominal fistula or gastrointestinal perforation within 6 months prior to
Day 1

25. Serious, non-healing wound, active ulcer, or untreated bone fracture

26. Proteinuria at Screening. Subjects with a urine dipstick protein ≥ 2+ at Screening
will undergo a 24-hour urine collection and must demonstrate ≤ 1g of protein in 24
hours to be eligible.

27. Known hypersensitivity to any inactive ingredient of bevacizumab

28. Known hypersensitivity to any inactive ingredient of TPI 287

29. Pregnancy (positive pregnancy test) or lactation

30. Inability to comply with protocol or study procedures

31. Previously or currently enrolled in Protocol No. TPI-287-17