A Phase 1, Open-Label, Dose Escalation, and Cohort Expansion Study to Evaluate the Safety,
Tolerability, Pharmacokinetics (PK) and Clinical Activity of DT2216, an Antiapoptotic Protein
Targeted Degradation Compound, in Subjects with Relapsed or Refractory Malignancies
This study is an open-label, first-in-human, dose escalation study in subjects with
histologically or cytologically confirmed advanced or metastatic malignancies who are no
longer responsive to approved or accepted standard-of-care interventions. The study will
consist of a dose escalation phase followed by confirmation of the recommended phase 2 dose
(RP2D).
Potentially eligible subjects will undergo screening evaluations (up to 28 days prior to
study therapy) and those who meet all protocol-defined eligibility criteria will be enrolled
into the study. Subjects who fail screening may be re-screened one time following correction
or mitigation of the condition that caused the screen failure; there is no time limit on when
a subject may be re-screened. Enrolled subjects will receive a single intravenous (IV)
infusion of study drug on Days 1 and 4 weekly for at least 4 weeks, with each cycle
consisting of 28 days. Treatment duration for an individual subject may continue for a
maximum of 1 year, until disease progression, unacceptable toxicity, subject withdrawal,
Investigator's decision for a change in treatment strategy for the individual subject, or
death. Longer therapy may be considered for individual subjects upon consultation with the
Sponsor's Medical Monitor and overall assessment of benefit:risk. Subjects will be followed
for safety for 28 days following the administration of the last study treatment.
Inclusion Criteria:
1. Adults aged 18 years or older on the day of signing informed consent.
2. Provide written informed consent for the trial, including willingness to comply with
all study related requirements.
3. Histologically or cytologically confirmed solid tumor. Subjects with more than 1
primary malignancy may be considered upon review with the Sponsor's Medical Monitor
4. Evidence of disease progression or inadequate response on the last regimen as assessed
by the Investigator.
5. Has exhausted all curative options or has a contraindication to approved therapies or
generally recognized standard-of-care measures for the subject's cancer.
6. Presence of measurable disease as assessed by the Investigator per Response Evaluation
Criteria in Solid Tumors (RECIST) 1.1
7. Have Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
8. Has adequate organ functions as defined by the following laboratory parameters at
baseline (laboratory parameters outside of these ranges that are deemed clinically
insignificant should be discussed with the Medical Monitor): (a) Absolute neutrophil
count ≥1.5 x 109/L; (b) hemoglobin ≥9 g/dL; (c) platelet count ≥100,000/mm3; (d)
aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤2.5 x upper limit
of normal (ULN); (e) total bilirubin ≤ 1.5 x institutional ULN (exception: subjects
with known Gilbert's syndrome and total bilirubin ≤3.0 x ULN at screening or anytime
during the prior 6 months are eligible); (f) c) adequate renal function defined as
calculated creatinine clearance >60 mL/min using the Cockcroft-Gault Method (Appendix
3); (g) acceptable coagulation parameters including international normalized ratio
(INR) <1.5 and partial thromboplastin time (PTT) ≤ institutional ULN; (h) serum
albumin ≥3.0 g/dL.
9. Left ventricular ejection fraction of ≥50% as assessed by echocardiogram or
multi-gated acquisition (MUGA) scan.
10. Adequate washout from the following prior to first dose of study therapy: Palliative
radiation ≥ 2 weeks; chemotherapy or targeted therapy ≥ 3 weeks or 5 half-lives;
biologic therapy ≥ 4 weeks.
11. Resolution to Grade ≤1 by the National Cancer Institute CTCAE, Version 5.0 (NCI-CTCAE
v 5.0) of all clinically significant toxic effects of prior therapies.
12. Female subjects: A female subject is eligible to participate if she is not pregnant,
not breastfeeding, and at least one of the following conditions applies: (a) Not a
woman of childbearing potential (WOCBP); (b) WOCBP who agrees to follow the
contraceptive guidance during the study treatment period and for at least 120 days
after the last dose of study treatment.
13. Female subject of childbearing potential must have a negative urine or serum pregnancy
test within 72 hours prior to receiving any dose of study medication. If the urine
test is positive or cannot be confirmed as negative, a serum pregnancy test will be
required.
14. Male subject is eligible to participate if he agrees to follow the acceptable
contraceptive guidance during the study treatment period and for at least 120 days
after the last dose of study treatment.
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Exclusion Criteria:
Diagnosis and Main Criteria for Inclusion:
Subjects are eligible to be included in the study only if all of the following criteria are
met:
Inclusion Criteria
1. Adults aged 18 years or older on the day of signing informed consent.
2. Provide written informed consent for the trial, including willingness to comply with
all study related requirements.
3. Histologically or cytologically confirmed solid tumor. Subjects with more than 1
primary malignancy may be considered upon review with the Sponsor's Medical Monitor.
4. Evidence of disease progression or inadequate response on the last regimen as assessed
by the Investigator.
5. Has exhausted all curative options or has a contraindication to approved therapies or
generally recognized standard-of-care measures for the subject's cancer.
6. Presence of measurable disease as assessed by the Investigator per Response Evaluation
Criteria in Solid Tumors (RECIST) 1.1
7. Have Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
8. Has adequate organ functions as defined by the following laboratory parameters at
baseline (laboratory parameters outside of these ranges that are deemed clinically
insignificant should be discussed with the Medical Monitor): (a) Absolute neutrophil
count ≥1.5 x 109/L; (b) hemoglobin ≥9 g/dL; (c) platelet count ≥100,000/mm3; (d)
aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤2.5 x upper limit
of normal (ULN); (e) total bilirubin ≤ 1.5 x institutional ULN (exception: subjects
with known Gilbert's syndrome and total bilirubin ≤3.0 x ULN at screening or anytime
during the prior 6 months are eligible); (f) c) adequate renal function defined as
calculated creatinine clearance >60 mL/min using the Cockcroft-Gault Method (Appendix
3); (g) acceptable coagulation parameters including international normalized ratio
(INR) <1.5 and partial thromboplastin time (PTT) ≤ institutional ULN; (h) serum
albumin ≥3.0 g/dL.
9. Left ventricular ejection fraction of ≥50% as assessed by echocardiogram or MUGA scan.
10. Adequate washout from the following prior to first dose of study therapy: Palliative
radiation ≥ 2 weeks; chemotherapy or targeted therapy ≥ 3 weeks or 5 half-lives;
biologic therapy ≥ 4 weeks.
11. Resolution to Grade ≤1 by the National Cancer Institute CTCAE, Version 5.0 (NCI-CTCAE
v 5.0) of all clinically significant toxic effects of prior therapies.
12. Female subjects: A female subject is eligible to participate if she is not pregnant,
not breastfeeding, and at least one of the following conditions applies: (a) Not a
woman of childbearing potential (WOCBP); (b) WOCBP who agrees to follow the
contraceptive guidance during the study treatment period and for at least 120 days
after the last dose of study treatment.
13. Female subject of childbearing potential must have a negative urine or serum pregnancy
test within 72 hours prior to receiving any dose of study medication. If the urine
test is positive or cannot be confirmed as negative, a serum pregnancy test will be
required.
14. Male subject is eligible to participate if he agrees to follow the acceptable
contraceptive guidance during the study treatment period and for at least 120 days
after the last dose of study treatment.
Exclusion Criteria
1. Received any BCL-XL directed therapy.
2. Administration of any blood products within the 30 days preceding the planned
administration of study therapy.
3. History of clinically significant bleeding and/or bleeding predisposition.
4. Significant liver insufficiency defined as Child-Pugh Class B or C
5. Concurrent administration of medications or foods that are strong inhibitors or
inducers of cytochrome P450 3A (CYP3A). Strong CYP3A inhibitors and inducers should be
discontinued at least 2 weeks prior to the first dose of DT2216 (Appendix 5).
6. Known active central nervous system (CNS) metastases/and or carcinomatous meningitis.
Subjects with previously treated brain metastases may participate provided they are
stable without evidence of progression via imaging for at least 4 weeks prior to first
dose of study therapy, are not receiving pharmacologic doses of glucocorticoids and
are without evidence of neurological symptoms. Carcinomatous meningitis is excluded
regardless of clinical stability.
7. Requiring anticoagulation for any reason (subjects who are on anticoagulants during
the screening period and are candidates for discontinuation can be considered).
8. Prior organ transplantation including allogeneic or autologous stem-cell
transplantation or other cellular therapies (e.g. chimeric antigen receptor T-cells
[CAR-T]).
9. Major surgery <4 weeks prior to first dose of study therapy.
10. Growth factor use <4 weeks prior to first dose of study therapy.
11. Participation in another research study involving receipt of an investigational
product <4 weeks prior to first dose of study therapy. If the half-life of the
investigational study is known, a shorter interval may be appropriate and should be
discussed with the Sponsor's Medical Monitor. Participants who have entered the
follow-up phase of an investigational study may be eligible as long as it has been 4
weeks after the last dose of the previous investigational agent.
12. Active autoimmune disease or history of chronic recurrent autoimmune disease,
requiring systemic treatment for the past 2 years (i.e. disease modifying agents,
corticosteroids or immunosuppressive drugs). Hormone replacement therapy (thyroxine,
insulin, or physiological corticosteroid replacement for either adrenal or pituitary
insufficiency) is not considered a form of systemic treatment directed at an
autoimmune disorder.
13. Systemic steroid therapy (>10 mg daily prednisone or equivalent) or any other form of
immunosuppressive therapy within 7 days prior to the first dose of study treatment
(note: topical, inhaled, nasal and ophthalmic steroids are permitted).
14. Known active hepatitis B (e.g, HBsAg reactive), hepatitis C (HCV) (e.g., HCV RNA
[qualitative] is detected). Subjects who have completed a course of anti-viral therapy
for hepatitis C and are polymerase chain reaction (PCR) negative are eligible.
15. Active infection with human immunodeficiency virus (HIV) unless: (a) Subject is
currently off antiretroviral therapy (ART) for at least 4 weeks; (b) HIV viral load of
< 400 copies per milliliter (/mL) at Screening (or undetectable per local criteria);
(c) cluster of differentiation (CD4) counts ≥200/microliter
16. Active infection requiring systemic therapy.
17. Known allergy to any component of the study treatment formulation(s).
18. Known history of marked prolongation of the QT or QT corrected (QT /QTc) interval or a
mean QTc as assessed by Fridericia's method (QTcF) value >470 msec following 3 ECG
determinations 5 minutes apart at Screening.
19. History of additional risk factors for Torsade de Pointes (including heart failure,
hypokalemia, family history of Long QT Syndrome, and use of concomitant medications
that prolong the QT/QTc interval.
20. Pregnant or breastfeeding or expecting to conceive or father children within the
projected duration of the trial, starting with the pre-screening or screening visit
through 120 days after the last dose of study treatment.
21. Clinically significant cardiovascular disease including: History of myocardial
infarction within 6 months prior to day 1 of study therapy, symptomatic congestive
heart failure (New York Heart Association Class II to IV), unstable angina, or serious
cardiac arrhythmia requiring treatment, uncontrolled angina within 3 months of day 1
of study therapy, uncontrolled hypertension.
22. Corona Virus Disease (COVID-19) diagnosis within 3 months of first dose of study drug.
23. Any other history of clinically significant and ongoing chronic respiratory disease,
gastrointestinal disease, liver disease, renal disease, endocrine disorder or any
other medical or psychiatric condition that in the opinion of the Investigator will
significantly increase the safety risk for the subject or confound the interpretation
of the study data.
24. History of alcohol or drug abuse within 6 months of first dose of study therapy or a
social situation that would interfere with the subject's participation in the trial.
25. In the opinion of the Investigator, participant has rapidly progressing disease, OR
has life expectancy <3 months.
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