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PARP Inhibitor BGB-290

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins · Phase 1 active Small molecule ✓ Verified May 2026 Quality 15/100

PARP Inhibitor BGB-290 is a Small molecule drug developed by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins. It is currently in Phase 1 development. Also known as: BGB-290, PARP, Inhibitor BGB-290, BGB-290, Pamiparib.

BGB-290, also known as pamiparib, is a small molecule inhibitor of the Poly [ADP-ribose] polymerase 1 (PARP1) enzyme. It is being studied in clinical trials for various conditions, including solid tumors, metastatic castration-resistant prostate cancer, and non-small-cell lung cancer.

Likelihood of approval
9.6% vs 9.6% industry baseline
If approved by FDA: likely 2033–2036
Steps remaining: Phase 2 → Phase 3 → NDA/BLA submission
Confidence: Medium
Why this estimate
  • Baseline phase 1 → approval rate +9.6pp
    Industry-wide phase 1 drugs reach approval ~9.6% of the time (BIO/Informa 2023 industry benchmark across all therapeutic areas).
Predicted approval windows by jurisdiction (conditional on FDA approval)
Regulator Country Likely year Lag vs FDA
FDA US 2033–2036
EMA EU 2034–2037 +0.7 yr
MHRA GB 2034–2037 +0.7 yr
Health Canada CA 2034–2038 +0.9 yr
TGA AU 2034–2038 +1.2 yr
PMDA JP 2034–2038 +1.5 yr
NMPA CN 2035–2039 +2.3 yr
MFDS KR 2034–2038 +1.4 yr
CDSCO IN 2034–2039 +1.8 yr
ANVISA BR 2035–2039 +2.3 yr

Hover any row for the lag rationale. Lag estimates are reduced when the drug has FDA Breakthrough or EMA PRIME designation (sponsors file globally in parallel).

Estimate based on the BIO/Informa industry phase transition rates plus per-drug modifiers for therapeutic area, sponsor type, FDA designations, mechanism, and trial design. Per-jurisdiction lags from Tufts CSDD international approval studies. Not investment, clinical or regulatory advice. Methodology: /methodology#likelihood.

At a glance

Generic namePARP Inhibitor BGB-290
Also known asBGB-290, PARP, Inhibitor BGB-290, BGB-290, Pamiparib
SponsorSidney Kimmel Comprehensive Cancer Center at Johns Hopkins
ModalitySmall molecule
PhasePhase 1

Approved indications

No approved indications tracked.

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:

Frequently asked questions about PARP Inhibitor BGB-290

What is PARP Inhibitor BGB-290?

PARP Inhibitor BGB-290 is a Small molecule drug developed by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins.

Who makes PARP Inhibitor BGB-290?

PARP Inhibitor BGB-290 is developed by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins (see full Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins pipeline at /company/sidney-kimmel-comprehensive-cancer-center-at-johns-hopkins).

Is PARP Inhibitor BGB-290 also known as anything else?

PARP Inhibitor BGB-290 is also known as BGB-290, PARP, Inhibitor BGB-290, BGB-290, Pamiparib.

What development phase is PARP Inhibitor BGB-290 in?

PARP Inhibitor BGB-290 is in Phase 1.

What are the side effects of PARP Inhibitor BGB-290?

Common side effects of PARP Inhibitor BGB-290 include Fatigue, Lymphocyte count decreased, Neutrophil count decreased, White blood cell decreased, Gastroesophageal Acid Reflux, anemia.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing