Biotech Brief
Catalyst Intelligence

Searchable Biotech Catalyst Intelligence

591 upcoming catalysts — clinical readouts, PDUFA dates, FDA decisions, and conference data cuts — ranked by importance and searchable by company, asset, or therapeutic area. 8 verified · 583 live-sourced.

591 catalysts · showing first 25
VKTX·VK2735 (oral)
Market Moving
Clinical ReadoutMetabolicPhase 3

Obesity

ExpectedQ3 2026· Confirmed
PoSProbability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
65%
Why It Matters

Oral GLP-1 competing directly with Lilly and Novo. Best-in-class efficacy in Phase 2 at ~15% weight loss. Phase 3 success could make Viking an M&A target.

VerifiedDetails →VerifiedEditor-reviewed catalyst with confirmed or carefully validated timing, source context, and executive summary.
REGN·Dupixent (IL-4Rα)
Market Moving
FDA DecisionRespiratoryRegistration

COPD

ExpectedQ3 2026· Confirmed
PoSProbability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
80%
Why It Matters

First biologic approved for COPD would open a massive new market. Commercial peak sales estimates of $3B+ annually. Eosinophilic COPD subgroup most likely to benefit.

VerifiedDetails →VerifiedEditor-reviewed catalyst with confirmed or carefully validated timing, source context, and executive summary.
LLY·Tirzepatide
Important
Clinical ReadoutCardiovascularPhase 3

Heart Failure with Preserved EF

ExpectedH2 2026· Confirmed
PoSProbability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
60%
Why It Matters

HFpEF has no approved pharmacological treatments. Positive data would expand GLP-1 addressable market substantially and reinforce cardiovascular benefits beyond weight loss.

VerifiedDetails →VerifiedEditor-reviewed catalyst with confirmed or carefully validated timing, source context, and executive summary.
·Xanamem
Important
Clinical ReadoutCNSPhase 2/Phase 3

Dementia Moderate

ExpectedQ4 2026· Est.
PoSest.Probability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
52%

Effect of 10 mg Xanamem on Dementia Due to Alzheimer's Disease

ClinicalTrials.govDetails →Live-SourcedPulled from public data sources and refreshed periodically. Timing and details should be independently verified.
·BHV-7000
Important
Clinical ReadoutCNSPhase 2/Phase 3

Focal Epilepsy

ExpectedQ4 2026· Est.
PoSest.Probability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
52%

Study to Determine if BHV-7000 is Effective and Safe in Adults With Refractory Focal Onset Epilepsy

ClinicalTrials.govDetails →Live-SourcedPulled from public data sources and refreshed periodically. Timing and details should be independently verified.
·Abiraterone - Usual
Important
Clinical ReadoutOncologyPhase 2/Phase 3

Prostate Cancer

ExpectedQ4 2026· Est.
PoSest.Probability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
52%

Pharmacogenomics IND Commercial SNP Clinical Study - Abiraterone and Single Nucleotide Polymorphisms

ClinicalTrials.govDetails →Live-SourcedPulled from public data sources and refreshed periodically. Timing and details should be independently verified.
·ETOPOSIDE - Usual
Important
Clinical ReadoutOncologyPhase 2/Phase 3

Small Cell Lung Cancer

ExpectedQ4 2026· Est.
PoSest.Probability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
52%

Pharmacogenomics ANDA SNP Clinical Study - Etoposide and Single Nucleotide Polymorphisms

ClinicalTrials.govDetails →Live-SourcedPulled from public data sources and refreshed periodically. Timing and details should be independently verified.
·ALECENSA - alectinib hydrochloride capsule
Important
Clinical ReadoutOncologyPhase 2/Phase 3

ALK-Positive Non-Small Cell Lung Cancer (NSCLC)

ExpectedQ4 2026· Est.
PoSest.Probability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
52%

Pharmacogenomics IND SNP Clinical Trial - Alectinib and Single Nucleotide Polymorphisms

ClinicalTrials.govDetails →Live-SourcedPulled from public data sources and refreshed periodically. Timing and details should be independently verified.
·Selinexor (combination therapy)
Important
Clinical ReadoutOncologyPhase 2/Phase 3

Relapsed/Refractory Diffuse Large B-cell Lymphoma

ExpectedQ4 2026· Est.
PoSest.Probability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
52%

A Study of Rituximab-Gemcitabine-Dexamethasone-Platinum (R-GDP) With or Without Selinexor in Patients With Relapsed/Refractory Diffuse Large B-cell Lymphoma

ClinicalTrials.govDetails →Live-SourcedPulled from public data sources and refreshed periodically. Timing and details should be independently verified.
·Raloxifene - Usual
Important
Clinical ReadoutOncologyPhase 2/Phase 3

Breast Cancer

ExpectedQ4 2026· Est.
PoSest.Probability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
52%

Bioequivalence ANDA SNP Clinical Study - Raloxifene and Single Nucleotide Polymorphisms

ClinicalTrials.govDetails →Live-SourcedPulled from public data sources and refreshed periodically. Timing and details should be independently verified.
·Durvalumab
Important
Clinical ReadoutOncologyPhase 3

Hepatocellular Carcinoma

ExpectedQ3 2026· Est.
PoSest.Probability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
52%

Durvalumab Plus Tremelimumab as First-line Treatment in Chinese Patients With uHCC

ClinicalTrials.govDetails →Live-SourcedPulled from public data sources and refreshed periodically. Timing and details should be independently verified.
·Durvalumab
Important
Clinical ReadoutOncologyPhase 3

Non-Small Cell Lung Cancer

ExpectedQ3 2026· Est.
PoSest.Probability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
52%

A Global Study to Assess the Effects of Durvalumab With Oleclumab or Durvalumab With Monalizumab Following Concurrent Chemoradiation in Patients With Stage III Unresectable Non-Small Cell Lung Cancer

ClinicalTrials.govDetails →Live-SourcedPulled from public data sources and refreshed periodically. Timing and details should be independently verified.
·Zanidatamab
Important
Clinical ReadoutOncologyPhase 3

Gastric Neoplasms

ExpectedQ3 2026· Est.
PoSest.Probability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
52%

A Study of Zanidatamab in Combination With Chemotherapy Plus or Minus Tislelizumab in Patients With HER2-positive Advanced or Metastatic Gastric and Esophageal Cancers

ClinicalTrials.govDetails →Live-SourcedPulled from public data sources and refreshed periodically. Timing and details should be independently verified.
·Entrectinib
Important
Clinical ReadoutOncologyPhase 3

Carcinoma, Non-Small-Cell Lung

ExpectedQ3 2026· Est.
PoSest.Probability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
52%

A Study to Compare the Efficacy and Safety of Entrectinib and Crizotinib in Participants With Advanced or Metastatic ROS1 Non-small Cell Lung Cancer (NSCLC) With and Without Central Nervous System (CNS) Metastases

ClinicalTrials.govDetails →Live-SourcedPulled from public data sources and refreshed periodically. Timing and details should be independently verified.
·Pemetrexed
Important
Clinical ReadoutOncologyPhase 3

Non-Small Cell Lung Cancer

ExpectedQ3 2026· Est.
PoSest.Probability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
52%

Neoadjuvant and Adjuvant Therapy Studies of Sindilizumab in Resectable Lung Cancer

ClinicalTrials.govDetails →Live-SourcedPulled from public data sources and refreshed periodically. Timing and details should be independently verified.
·[O-15]-Water PET Myocardial Perfusion Imaging (MPI)
Important
Clinical ReadoutCardiovascularPhase 3

Coronary Artery Disease

ExpectedQ4 2026· Est.
PoSest.Probability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
56%

RAdiolabeled Perfusion to Identify Coronary Artery Disease Using WAter To Evaluate Responses of Myocardial FLOW (RAPID-WATER-FLOW)

ClinicalTrials.govDetails →Live-SourcedPulled from public data sources and refreshed periodically. Timing and details should be independently verified.
·AK112, Gemcitabine, Cisplatin
Important
Clinical ReadoutOncologyPhase 3

Biliary Tract Cancer

ExpectedQ4 2026· Est.
PoSest.Probability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
52%

AK112 Combined With Chemotherapy Versus Durvalumab Combined With Chemotherapy in Advanced Biliary Tract Cancer

ClinicalTrials.govDetails →Live-SourcedPulled from public data sources and refreshed periodically. Timing and details should be independently verified.
·Pirtobrutinib
Important
Clinical ReadoutOncologyPhase 3

Chronic Lymphocytic Leukemia

ExpectedQ4 2026· Est.
PoSest.Probability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
52%

A Trial of Pirtobrutinib (LOXO-305) Plus Venetoclax and Rituximab (PVR) Versus Venetoclax and Rituximab (VR) in Previously Treated Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma (CLL/SLL)

ClinicalTrials.govDetails →Live-SourcedPulled from public data sources and refreshed periodically. Timing and details should be independently verified.
·BL-M07D1
Important
Clinical ReadoutOncologyPhase 3

HER2-positive Breast Cancer

ExpectedQ4 2026· Est.
PoSest.Probability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
52%

A Study Comparing BL-M07D1 With T-DM1 in Patients With Unresectable Locally Advanced or Metastatic HER2-positive Breast Cancer

ClinicalTrials.govDetails →Live-SourcedPulled from public data sources and refreshed periodically. Timing and details should be independently verified.
·Ziltivekimab
Important
Clinical ReadoutCardiovascularPhase 3

Heart Failure

ExpectedQ4 2026· Est.
PoSest.Probability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
56%

A Research Study Looking Into How Ziltivekimab Works Compared to Placebo in Participants With Heart Failure and Inflammation

ClinicalTrials.govDetails →Live-SourcedPulled from public data sources and refreshed periodically. Timing and details should be independently verified.
·Apalutamide
Important
Clinical ReadoutOncologyPhase 3

Metastatic Castrate-sensitive Prostate Cancer

ExpectedQ4 2026· Est.
PoSest.Probability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
52%

A Study of an Intermittent ADT Approach With Apalutamide Monotherapy in Participants With mCSPC

ClinicalTrials.govDetails →Live-SourcedPulled from public data sources and refreshed periodically. Timing and details should be independently verified.
·Atezolizumab
Important
Clinical ReadoutOncologyPhase 3

Unresectable Hepatocellular Carcinoma

ExpectedQ4 2026· Est.
PoSest.Probability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
52%

A Study of Atezolizumab With Lenvatinib or Sorafenib Versus Lenvatinib or Sorafenib Alone in Hepatocellular Carcinoma Previously Treated With Atezolizumab and Bevacizumab

ClinicalTrials.govDetails →Live-SourcedPulled from public data sources and refreshed periodically. Timing and details should be independently verified.
·Milvexian
Important
Clinical ReadoutCardiovascularPhase 3

Ischemic Stroke; Ischemic Attack, Transient

ExpectedQ4 2026· Est.
PoSest.Probability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
56%

A Study of Milvexian in Participants After an Acute Ischemic Stroke or High-Risk Transient Ischemic Attack- LIBREXIA-STROKE

ClinicalTrials.govDetails →Live-SourcedPulled from public data sources and refreshed periodically. Timing and details should be independently verified.
·Ocrelizumab
Important
Clinical ReadoutCNSPhase 3

Progressive Multiple Sclerosis (PMS)

ExpectedQ4 2026· Est.
PoSest.Probability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
52%

A Study to Evaluate Ocrelizumab Treatment in Participants With Progressive Multiple Sclerosis

ClinicalTrials.govDetails →Live-SourcedPulled from public data sources and refreshed periodically. Timing and details should be independently verified.
·Inclisiran sodium 300 mg
Important
Clinical ReadoutCardiovascularPhase 3

Coronary Artery Disease

ExpectedQ4 2026· Est.
PoSest.Probability of Success — illustrative analyst consensus estimate. Not primary research. Always verify with company filings, ClinicalTrials.gov, and FDA.gov.
56%

Coronary Computed Tomography Study to Assess the Effect of Inclisiran in Addition to Maximally Tolerated Statin Therapy on Atherosclerotic Plaque Progression in Participants With a Diagnosis of Non-obstructive Coronary Artery Disease Without Previous Cardiovascular Events

ClinicalTrials.govDetails →Live-SourcedPulled from public data sources and refreshed periodically. Timing and details should be independently verified.

Verified: Editor-reviewed catalyst with validated timing, source context, and executive summary.

Live-Sourced: Pulled from public data sources and refreshed periodically. Timing and details should be independently verified.

PoS estimates are illustrative figures based on BIO/IQVIA phase benchmarks — not primary research. Click any catalyst to view full program details.