Pipeline dossier

NIH & clinical-trial pipeline signals for ASTRAZENECA PLC (AZN)

Leading indicators across the NIH grant → clinical trial → SEC filing chain for AZN, mapped to public ticker AZN (CIK 0000901832). Sourced live from public data.

⚠ Research/informational signals from public data (NIH · ClinicalTrials.gov · SEC EDGAR). Not investment advice. Full scope →
Trial → FilingAZN55% conf

ASTRAZENECA PLC (AZN) — PHASE1 primary completion in ~105 days

Upstream (observed)
Clinical trial status (PHASE1) — A Study to Investigate the Relative Bioavailability and Safety of Different Oral Formulations of Elecoglipron in Healthy Participants
↓ Phase-transition base rate 52% (Wong/Siah/Lo 2019)
Predicted downstream
SEC 8-K / press release on Phase 2 readout / advance (12-24 mo, base rate 52%)
Trial → FilingAZN55% conf

ASTRAZENECA PLC (AZN) — trial primary completion in ~57 days

Upstream (observed)
Clinical trial status (n/a) — A Pan-European Post-Authorisation Safety Study: Risk of Pancreatic Cancer Among Type 2 Diabetes Patients Who Initiated Exenatide as Compared With Those Who Initiated Other Non-Glucagon-Like Peptide 1 Receptor Agonists Based Glucose Lowering Drugs
↓ days–weeks to disclosure
Predicted downstream
SEC 8-K / press release (material trial update) (days–weeks)
Trial → FilingAZN55% conf

ASTRAZENECA PLC (AZN) — PHASE1 primary completion in ~177 days

Upstream (observed)
Clinical trial status (PHASE1) — A Study to Investigate the Efficacy and Safety of Volrustomig ± Casdatifan vs Nivolumab + Ipilimumab as 1L Treatment for Advanced ccRCC
↓ Phase-transition base rate 52% (Wong/Siah/Lo 2019)
Predicted downstream
SEC 8-K / press release on Phase 2 readout / advance (12-24 mo, base rate 52%)
Trial → FilingAZN35% conf

ASTRAZENECA PLC (AZN) — trial protocol updated 1 days ago

Upstream (observed)
Clinical trial status (n/a) — Durvalumab Consolidation After Chemoradiation Therapy for Limited Stage SCLC in China
↓ days–weeks to disclosure
Predicted downstream
SEC 8-K / press release (material trial update) (days–weeks)
Trial → FilingAZN35% conf

ASTRAZENECA PLC (AZN) — trial protocol updated 1 days ago

Upstream (observed)
Clinical trial status (n/a) — A Real-world Study Observing Treatment Patterns and Clinical Results for Patients in China With Hormone Receptor-positive, HER2-negative Metastatic Breast Cancer.
↓ days–weeks to disclosure
Predicted downstream
SEC 8-K / press release (material trial update) (days–weeks)
Trial → FilingAZN35% conf

ASTRAZENECA PLC (AZN) — PHASE3 protocol updated 1 days ago

Upstream (observed)
Clinical trial status (PHASE3) — A Phase III Study to Investigate the Efficacy and Safety of Elecoglipron Compared With Placebo in Adults With Type 2 Diabetes Mellitus on Background Insulin
↓ Phase-transition base rate 57% (Wong/Siah/Lo 2019)
Predicted downstream
SEC 8-K / press release on NDA/BLA filing (FDA submission) (12-24 mo, base rate 57%)
Trial → FilingAZN35% conf

ASTRAZENECA PLC (AZN) — PHASE3 protocol updated 1 days ago

Upstream (observed)
Clinical trial status (PHASE3) — A Phase III Study to Investigate the Efficacy and Safety of Elecoglipron Alone or in Combination With Dapagliflozin Compared With Placebo in Adults With Type 2 Diabetes Mellitus
↓ Phase-transition base rate 57% (Wong/Siah/Lo 2019)
Predicted downstream
SEC 8-K / press release on NDA/BLA filing (FDA submission) (12-24 mo, base rate 57%)
Trial → FilingAZN35% conf

ASTRAZENECA PLC (AZN) — PHASE3 protocol updated 1 days ago

Upstream (observed)
Clinical trial status (PHASE3) — A Phase III Study to Investigate the Efficacy and Safety of Elecoglipron Compared With Placebo in Adults With Type 2 Diabetes Mellitus and Impaired Renal Function on Background Dapagliflozin
↓ Phase-transition base rate 57% (Wong/Siah/Lo 2019)
Predicted downstream
SEC 8-K / press release on NDA/BLA filing (FDA submission) (12-24 mo, base rate 57%)
Trial → FilingAZN35% conf

ASTRAZENECA PLC (AZN) — PHASE3 protocol updated 1 days ago

Upstream (observed)
Clinical trial status (PHASE3) — A Phase III Study to Investigate the Efficacy and Safety of the Combination of Elecoglipron and Dapagliflozin in Adults With Type 2 Diabetes Mellitus
↓ Phase-transition base rate 57% (Wong/Siah/Lo 2019)
Predicted downstream
SEC 8-K / press release on NDA/BLA filing (FDA submission) (12-24 mo, base rate 57%)

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