An Open-label, Phase I/IIa, Dose Escalating Study of 2B3-101 in Patients With Solid Tumors and Brain Metastases or Recurrent Malignant Glioma.

This is a Phase I/IIa, multicenter, open-label, dose-escalation study. The study will be
conducted in 6 phases: "2B3-101 single agent dose-escalation phase", "a 2B3-101 with
trastuzumab dose-escalation phase", "a Breast cancer brain metastases study-expansion
phase","a Recurrent malignant glioma study-expansion phase", "a Melanoma brain metastases
study- expansion phase" and "SCLC brain metastases study-expansion phase"

2B3-101 single agent dose-escalation phase.

In the 2B3-101 single Agent dose-escalation phase, female and male patients with solid
tumors and brain metastases or recurrent malignant glioma will be enrolled. Patients will be
assigned to a dose level cohort. - The starting dose will be 5 mg/m2, which is equal to 1/10
of the human equivalent dose of the LD10 of 2B3-101 in rats. A "3+3" dose-escalation design
will be used. The study will investigate sequential cohorts consisting of 3-6 patients to be
enrolled and treated at the applicable dose level. Planned dose levels for subsequent
cohorts are 10, 20, 30, mg/m2 and steps of 10 mg/m2 thereafter. For more information on the
dose escalation design and the increments, please see the dose escalation criteria section.

There will be no intra-patient dose escalation. Each treatment cycle consists of 21 days.
Patients will receive a single IV dose of 2B3-101 on day 1 of each cycle. In order to
minimize the risk of infusion reactions 5% of the total dose of 2B3-101 (in mg) should be
infused slowly over the first 30 minutes. If tolerated, the infusion may then be completed
over the next hour for a total infusion time of 90 minutes. Blood samples will be taken on
day 1, 2, 3, 5, 8 and 11 of cycle 1 and day 1, 8 and 15 of cycle 2 to assess the PK profile
during the first 2 cycles. The dose limiting toxicity (DLT) observation period for each dose
level will be cycle 1 (day 1 to day 21). Patients who do not complete the DLT observation
period (cycle 1) for other reasons than a DLT will be replaced.

Once the MTD of 2B3-101 as single agent has been determined, the study will continue to the
breast cancer brain metastases and recurrent malignant glioma dose expansion phases.

2B3-101 in combination with trastuzumab dose-escalation phase

In the 2B3-101 in combination with trastuzumab dose escalation phase, only patients with
HER2+ breast cancer and brain metastases will be enrolled.

The patients will be assigned to a 2B3-101 dose level cohort. - The starting dose of 2B3-101
will be 40 mg/m2 every 3 weeks. This dose has been selected based upon safety information
from patients treated with 2B3-101 at this dose level, as well as upon previous treatment
with PEGylated liposomal doxorubicin in combinations trastuzumab (Chia et al 2006).

The dose-escalation will be conducted in steps of 10 mg/m2 up to the MTD level determined
for 2B3-101 as single agent. The trastuzumab dose will remain fixed to a loading dose of 8
mg/kg at day 1 and 6 mg/kg every 3 weeks at the subsequent cycles throughout the
determination of the MTD. Enrolment of HER2+ patients breast cancer patients in the "2B3-101
in combination with trastuzumab dose-escalation" phase of the study will be allowed in
parallel with the determination of the MTD of 2B3-101 as single agent. A "3+3"
dose-escalation design will be used. Thus, the study will investigate sequential cohorts of
3-6 patients, who will be enrolled and treated at the applicable dose levels.

No intra-patient dose-escalation will be allowed. Each treatment cycle consists of 21 days.
All patients will receive a single IV dose of 2B3-101 on day 1 of each cycle. In order to
minimize the risk of infusion reactions 5% of the total dose of 2B3-101 (in mg) should be
infused slowly over the first 30 minutes. As long as 2B3-101 is well tolerated, the
remaining 95% of the infusion could thereafter be administered over the next 60 min,
resulting in a total infusion time of 90 minutes. The infusion of trastuzumab will then
follow 30 minutes after the completion of the 2B3-101 infusion. Blood samples will be taken
on day 1, 2, 3, 5, 8 and 11 of cycle 1, on day 1, 8 and 15 of cycle 2 and if applicable on
day 1 of cycle 3 and day 1 of cycle 4 to assess the PK profile of 2B3-101 during the first 4
cycles. The dose limiting toxicity (DLT) observation period will be cycle 1 (day 1 to day
21) at each individual dose level. Patients who do not complete the DLT observation period
(cycle 1) for other reasons than a DLT will be replaced.

Breast cancer brain metastases expansion phase.

In the breast cancer brain metastases expansion phase, each treatment cycle consists of 21
days. Patients will receive a single IV dose of 2B3-101 on day 1 of each cycle. In order to
minimize the risk of infusion reactions 5% of the total dose of 2B3-101 (in mg) should be
infused slowly over the first 30 minutes. If tolerated, the infusion may then be completed
over the next hour for a total infusion time of 90 minutes. Blood samples will be taken on
day 1, 2, 3, 5, 8 and 11 of cycle 1 on day 1, 8 and 15 of cycle 2 and if applicable on day 1
of cycle 3 and on day 1 of cycle 4 to assess the PK profile during the first 4 cycles.

Recurrent malignant glioma expansion phase.

In the recurrent malignant glioma expansion phase, each treatment cycle is 28 days long.
Patients will receive a single IV dose of 2B3-101 on day 1 of each cycle. In order to
minimize the risk of infusion reactions 5% of the total dose of 2B3-101 (in mg) should be
infused slowly over the first 30 minutes. If tolerated, the infusion may then be completed
over the next hour for a total infusion time of 90 minutes. Blood samples will be taken on
day 1, 2, 3, 5, 8 and 11 of cycle 1, day 1, 8 and 15 of cycle 2 and if applicable on day 1
of cycle 3 and on day 1 of cycle 4 to assess the PK profile during the first 4 cycles.

SCLC brain metastases study arm of the expansion phase

In the SCLC brain metastases study arm of the expansion phase, each treatment cycle is 21
days long. Patients will receive a single IV dose of 2B3-101 at MTD determined for 2B3-101
as single agent on day 1 of each cycle. In order to minimize the risk of infusion reactions
5% of the total dose (in mg) should be infused slowly over the first 30 minutes. As long as
2B3-101 is well tolerated, the remaining 95% of the infusion could thereafter be
administered over the next 60 minutes, resulting in a total infusion time of 90 minutes.
Blood samples will be taken on day 1, 2, 3, 5, 8 and 11 of cycle 1, day 1, 8 and 15 of cycle
2 and if applicable on day 1 of cycle 3 and on day 1 of cycle 4 to assess the PK profile
during the first 4 cycles.

Melanoma brain metastases study arm of the expansion phase

In the melanoma brain metastases study arm of the expansion phase, each treatment cycle is
21 days long. Patients will receive a single IV dose of 2B3-101 at MTD determined for
2B3-101 as single agent in the dose escalation phase on day 1 of each cycle. In order to
minimize the risk of infusion reactions 5% of the total dose (in mg) should be infused
slowly over the first 30 minutes. As long as 2B3-101 is well tolerated, the remaining 95% of
the infusion could thereafter be administered over the next 60 minutes, resulting in a total
infusion time of 90 minutes. Blood samples will be taken on day 1, 2, 3, 5, 8 and 11 of
cycle 1, day 1, 8 and 15 of cycle 2 and if applicable on day 1 of cycle 3 and on day 1 of
cycle 4 to assess the PK profile during the first 4 cycles.

For all stages a patient will stay on treatment until disease progression, unacceptable
toxicity, or discontinuation for any other reason.

Inclusion Criteria:

1. Age ≥ 18 years.

2. Measurable intracranial disease by MRI.

3. ECOG Performance Status ≤ 2.

4. Estimated life expectancy of at least 8 weeks.

5. Toxicities incurred as a result of previous anticancer therapy (radiation therapy,
chemotherapy, or surgery) must be resolved to ≤ grade 2 (as defined by CTCAE version
4.0).

6. No evidence of (cortical) cognitive impairment as defined by a Mini-Mental Status
Exam (MMSE) score ≥ 25/30.

7. Written informed consent according to local guidelines.

In addition to the above listed eligibility criteria, the following criteria are
applicable:

8.

- 2B3-101 single agent dose-escalation phase:

1. Patients with pathologically confirmed diagnosis of advanced, recurrent solid
tumors and unequivocal evidence of brain metastases that are refractory to
standard therapy or for whom no standard therapy exists or with unequivocal
evidence of newly diagnosed untreated brain metastases and controlled
extracranial disease which per the multi-disciplinary team decision do not
require immediate radiotherapy, surgery or standard systematic chemotherapy.
Brain metastases may be stable, progressive, symptomatic or asymptomatic brain
metastasis/es. Stable or decreasing dosage of steroids (e.g. dexamethasone) for
7 days prior to baseline MRI or non-enzyme inducing anti-epileptic drugs is
allowed.

Or -

2. Patients with pathology confirmed diagnosis of advanced, recurrent primary
malignant (grade III and IV) glioma that are refractory to standard therapy or
for whom no standard therapy exists. Stable or decreasing dosage of steroids
(e.g. dexamethasone) for 7 days prior to baseline MRI or non-enzyme inducing
anti-epileptic drugs are allowed.

- 2B3-101 in combination with trastuzumab dose escalation phase:

Patients with histologically-confirmed HER2-positive (IHC 3+ or fluorescence in situ
hybridization [FISH] amplified; by clinical assay on either primary or metastatic tumor)
adenocarcinoma of the breast with unequivocal evidence of brain metastases that are
refractory to standard therapy or for which no standard therapy exist or with unequivocal
evidence of newly diagnosed untreated brain metastases and controlled extracranial disease
which per the multi-disciplinary team decision do not require immediate radiotherapy,
surgery or standard systematic chemotherapy can be included to this escalation phase as
well.

- Breast cancer brain metastases expansion phase:

1. Patients with pathologically confirmed diagnosis of advanced, recurrent breast cancer
with at least one progressive and/or new metastatic brain lesion, that are
refractory to standard therapy or for whom no standard therapy exist. Brain
metastases may be stable, progressive, symptomatic or asymptomatic brain
metastasis/es. Stable or decreasing dosage of steroids (e.g. dexamethasone) for 7
days prior to baseline MRI or non-enzyme inducing anti-epileptic drugs is allowed.

Or -

2. Patients with pathologically confirmed diagnosis of advanced breast cancer with newly
diagnosed, untreated, brain metastases and controlled extracranial disease which per
the multi-disciplinary team decision do not require immediate radiotherapy, surgery
or standard systematic chemotherapy.

SCLC brain metastases study arm of the expansion phase:

1. Patients with pathologically confirmed diagnosis of advanced, recurrent SCLC with at
least one progressive and/or new metastatic brain lesion that are refractory to
standard therapy or for whom no standard therapy exist. Stable or decreasing dosages
of steroids (e.g. dexamethasone) for 7 days prior to baseline MRI and/or use of
non-enzyme inducing anti-epileptic drugs are allowed.

Or

2. Patients with pathologically confirmed diagnosis of advanced SCLC with newly
diagnosed, untreated, brain metastases and controlled extracranial disease which per
the multi-disciplinary team decision do not require immediate radiotherapy, surgery
or standard systematic chemotherapy.

Melanoma brain metastases study arm of the expansion phase:

1. Patients with pathologically confirmed diagnosis of advanced, recurrent melanoma with
at least one progressive and/or new metastatic brain lesion that are refractory to
standard therapy or for whom no standard therapy exist. Stable or decreasing dosages
of steroids (e.g. dexamethasone) for 7 days prior to baseline MRI and/or use of
non-enzyme inducing anti-epileptic drugs are allowed.

Or

2. Patients with pathologically confirmed diagnosis of advanced melanoma with newly
diagnosed, untreated, brain metastases and controlled extracranial disease which per
the multi-disciplinary team decision do not require immediate radiotherapy, surgery
or standard systematic chemotherapy.

Recurrent malignant glioma study arm of the expansion phase:

1. 7 patients with histologically proven glioma grade IV, which is progressive following
first line treatment with surgery or biopsy followed by fractionated radiotherapy
with concurrent temozolomide-containing chemotherapy.

and

2. 7 patients with recurrent histologically confirmed malignant (WHO grade III and IV)
glioma or histologically confirmed low-grade (WHO grade II) glioma with radiographic
evidence of malignant transformation by MRI, that are refractory to standard therapy,
or for whom no standard therapy exists or do not require immediate standard therapy
per the multi-disciplinary team decision. Patients in both groups should have stable
or decreasing dosage of steroids (e.g. dexamethasone) for a minimum of 7 days prior
to baseline MRI. Non-enzyme inducing anti-epileptic drugs are allowed

Exclusion Criteria.

- Prior Treatment. 1. Less than 1 week since the last treatment of lapatinib, less
than 2 weeks since the last treatment of vemurafenib, less than 4 weeks since
the last treatment of chemotherapy, biological therapy, immunotherapy and
systemic radiotherapy (except palliative radiation delivered to <20% of bone
marrow), less than 8 weeks for cranial radiotherapy, and less than 6 weeks for
nitrosoureas and mitomycin C.

2. Patients that have received a maximum cumulative dose of free (i.e.,
non-liposomal) or liposomal doxorubicin > 360mg/m2 or free epirubicin >
600mg/m2.

- Current Treatment. 3. Current or recent (within 30 days of first study
treatment) treatment with another investigational drug or participation in
another investigational study.

- Hematology, coagulation and biochemistry. 4. Inadequate bone marrow function:
Absolute Neutrophil Count (ANC): < 1.5 x 109/L, or platelet count < 100 x 109/L
or hemoglobin < 6 mmol/L.

5. Inadequate liver function, defined as:

• Serum (total) bilirubin > 1.5 x the ULN for the institution if no liver
metastases (> 2 x ULN in patients with liver metastases);

• ASAT or ALAT > 2.5 x ULN if no liver metastases (> 4 x ULN in patients with
liver metastases);

- Alkaline phosphatase levels > 2.5 x ULN if no liver metastases (> 5 x ULN
in patients with liver metastases, or > 10 x ULN in patients with bone
metastases).

6. Inadequate renal function, defined as:

- Serum creatinine > 1.5 x ULN.

- Other. 7. Leptomeningeal carcinomatosis as the only site of CNS involvement. 8.
Pregnancy or lactation. Serum pregnancy test to be performed within 7 days prior
to study treatment start, or within 14 days followed by a confirmatory urine
pregnancy test within 7 days prior to study treatment start.

9. For female subjects of childbearing potential (defined as < 2 years after
last menstruation and not surgically sterile) and male subjects who are not
surgically sterile or with female partners of childbearing potential: absence of
effective, non-hormonal means of contraception (intrauterine contraceptive
device, barrier method of contraception in conjunction with spermicidal gel).

10. Major surgical procedure (including open biopsy, excluding central line IV
and portacath) within 28 days prior to the first study treatment, or
anticipation of the need for major surgery during the course of the study
treatment.

11. Grade 3 or 4 motor, sensory, or cranial neuropathy symptoms (as defined by
CTCAE version 4.0).

12. Uncontrolled hypertension (systolic > 150 mm Hg and/or diastolic > 100mm
Hg).

13. Clinically significant (i.e. active) cardiovascular disease defined as:

• Stroke within ≤ 6 months prior to day 1;

• Transient Ischemic Attack (TIA) within ≤ 6 months prior to day 1;

• Myocardial infarction within ≤ 6 months prior to day 1;

• Unstable angina;

- New York Heart Association (NYHA) Grade II or greater Congestive Heart
Failure (CHF);

- Serious cardiac arrhythmia requiring medication;

- Clinically relevant pathologic findings in ECG. 14. Left Ventricle Ejection
Fraction (LVEF) by MUGA or ECHO < 55% for patients receiving 2B3-101 in
combination with trastuzumab. For patients receiving single agent 2B3-101
treatment. Left Ventricle Ejection Fraction (LVEF) by MUGA or ECHO < 50%.

15. Known hypersensitivity to any of the study drugs excipients (e.g.
doxorubicin, PEG or GSH).

16. Evidence of any other medical conditions (such as psychiatric illness,
infectious diseases, physical examination or laboratory findings) that may
interfere with the planned treatment, affect patient compliance or place
the patient at high risk from treatment-related complications.