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CEP-18770

Phase 1

Multiple Myeloma | Small molecule | Oncology |Teva Pharmaceutical Industries Limited|Trials Updated: Jun 28, 2023

CEP-18770 development status

Highest phase Phase 1
Registered trials 2 across 2 sponsors since May 2011

CEP-18770 target and mechanism

ModalitySmall molecule

Also known as Delanzomib

Success Probability

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Market & Valuation

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Trial Design

CONTROLLED
Total Trials1
Total Enrollment11

FDA Designations

No designations recorded

CEP-18770 clinical trials

CEP-18770 · 1 trial · 1 indication

Phase 1 1
NCT01348919Delanzomib (CEP-18770) in Combination With Lenalidomide and Dexamethasone in Relapsed or Refractory Multiple MyelomaMultiple Myeloma
COMPLETED11 Analytics
PHASE1COMPLETED
Delanzomib (CEP-18770) in Combination With Lenalidomide and Dexamethasone in Relapsed or Refractory Multiple Myeloma
Multiple MyelomaUnlock trial analytics

Study Endpoints

Primary Endpoints

Overall Response Rate (ORR) in Participants Treated at the (Maximum Tolerated Dose) MTD, as Assessed Using International Myeloma Working Group (IMWG) Criteria
From the first administration of CEP-18770 up to approximately 1.5 years

The ORR is defined as percentage of participants who achieve a best response of stringent complete response (sCR), complete response (CR), very good partial response (VGPR), or partial response (PR) during the study. sCR: negative immunofixation in serum and urine; disappearance of any soft tissue plasmacytomas; \< 5% plasma cells in bone marrow; normal free light chain (FLC) ratio; and absence of clonal cells in bone marrow. CR: negative immunofixation in serum and urine; disappearance of any soft tissue plasmacytomas; and \<5% plasma cells in bone marrow. VGPR: serum and urine M-protein detectable by immunofixation but not on electrophoresis; 90% or greater reduction in serum M-protein level and urine M-protein level less than 100 milligrams (mg)/24 hours. PR: ≥50% reduction in serum M-protein level; ≥90% reduction in 24-hour urinary M-protein level or reduction to less than 200 mg per 24 hours; and ≥50% reduction in the size of any soft tissue plasmacytomas present at baseline.

Maximum Tolerated Dose of CEP-18770
Cycle 1 (28 days)

MTD was based on the assessment of dose-limiting toxicity (DLT) during cycle 1 only and was defined as the highest dose at which fewer than one-third of participants in a cohort experience DLT. A DLT was defined as any of the following drug-related toxicities occurring during Cycle 1: Hematologic adverse events (AEs) (Grade 4 hematologic AEs, Grade 3 hematologic AEs with sequelae); Grade 3 nonhematologic AEs; Neuropathy (Grade 2 neuropathy, Grade 1 neuropathy with pain, worsening grade of neuropathy or new symptoms of pain associated with neuropathy); Any other toxicity that, in the judgment of the principal investigator, was a DLT; If a participant cannot receive 75% of the planned dose for any of the 3 agents (missing \>1 dose of CEP-18770, or \>5 doses of lenalidomide, or \>1 dose of dexamethasone \[either consecutively or separately\]), due to a drug-related AE, the event was considered a DLT, even if the grade of toxicity was lower than specified DLT determination as described above.

Secondary Endpoints

Duration of Response (DOR) for Participants Treated With CEP-18770 at the MTD, as Assessed Using IMWG Criteria
From the date of first response to the date of disease progression (up to approximately 1.5 years)
Time to Progression (TTP) for Participants Treated With CEP-18770 at the MTD, as Assessed Using IMWG Criteria
From the date of first dose of study drug to the date of disease progression (up to approximately 1.5 years)
Number of Participants With Adverse Events (AEs)
From the first administration of CEP-18770 up to approximately 1.5 years
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Study Design & Arms

AllocationNON_RANDOMIZED
MaskingNONE
ModelSEQUENTIAL
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
CEP-18770 Dose AEXPERIMENTALParticipants will receive CEP-18770 Dose A intravenously (IV) on Days 1, 8, and 15 in each 28-day cycle. In addition, participants will receive a fixed dose of 25 mg oral lenalidomide on Days 1 through 21 and a fixed dose of 40 mg oral dexamethasone on Days 1, 8, 15, and 22 of each 28-day cycle.
CEP-18770 Dose BEXPERIMENTALParticipants will receive CEP-18770 Dose B IV on Days 1, 8, and 15 in each 28-day cycle. In addition, participants will receive a fixed dose of 25 mg oral lenalidomide on Days 1 through 21 and a fixed dose of 40 mg oral dexamethasone on Days 1, 8, 15, and 22 of each 28-day cycle.
CEP-18770 Dose CEXPERIMENTALParticipants will receive CEP-18770 Dose C IV on Days 1, 8, and 15 in each 28-day cycle. In addition, participants will receive a fixed dose of 25 mg oral lenalidomide on Days 1 through 21 and a fixed dose of 40 mg oral dexamethasone on Days 1, 8, 15, and 22 of each 28-day cycle.

Interventions

NameTypeDescription
CEP-18770DRUGCEP-18770 will be administered per dose and schedule specified in the arm description.
LenalidomideDRUGLenalidomide will be administered per dose and schedule specified in the arm description.
DexamethasoneDRUGDexamethasone will be administered per dose and schedule specified in the arm description.
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Eligibility Criteria

Age Range18 Years to N/A
SexALL
Healthy VolunteersNo
Study Sites8

Inclusion Criteria: * The participant is a man or woman at least 18 years of age with documented multiple myeloma. * The participant has relapsed or progressive disease after receiving at least 1 previous chemotherapy treatment but no more than 5 previous therapies. * The participant has measurable...

Countries:United StatesNew Zealand
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Competitive Landscape -Multiple Myeloma 338 trials

Frequently asked questions about CEP-18770

What is CEP-18770 used for?

CEP-18770 is an investigational small molecule being studied for the treatment of multiple myeloma. It is being developed by Teva Pharmaceutical Industries Limited (TEVA). The drug is currently in Phase 1 clinical development and is not yet approved by regulatory authorities.

What does CEP-18770 target?

CEP-18770 is a small molecule therapeutic being investigated for multiple myeloma. The specific molecular target of CEP-18770 has not been disclosed in available clinical trial information. The drug is in Phase 1 development by Teva Pharmaceutical Industries Limited (TEVA).

Who makes CEP-18770?

CEP-18770 is being developed by Teva Pharmaceutical Industries Limited, a company traded on the New York Stock Exchange under the ticker symbol TEVA. The drug is an investigational small molecule in Phase 1 clinical development for the treatment of multiple myeloma.

What phase is CEP-18770 in?

CEP-18770 is in Phase 1 clinical development. It is an investigational drug being studied for multiple myeloma and has not been approved by the FDA or other regulatory agencies. The drug is being developed by Teva Pharmaceutical Industries Limited (TEVA).

What clinical trials is CEP-18770 in?

CEP-18770 has one completed Phase 1 clinical trial, identified as NCT01348919. This trial studied delanzomib (CEP-18770) in combination with lenalidomide and dexamethasone in patients with relapsed or refractory multiple myeloma. The study enrolled 11 participants and was conducted in the United States and New Zealand.

Is CEP-18770 the same as delanzomib?

Yes, CEP-18770 is also known as delanzomib. In clinical trial NCT01348919, the drug is referred to as delanzomib (CEP-18770). This Phase 1 study evaluated the drug in combination with lenalidomide and dexamethasone for relapsed or refractory multiple myeloma.