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Innovent Biologics Inc/ADR

IVBXF
$19.21B
Large Cap
NASDAQBiotechnology🇺🇸North AmericaNEW YORK6.2K employees

Drugs in Pipeline

43

Phase 3 Programs

20

Upcoming Catalysts

10

Next Catalyst

This month

Market Overview

Stock performance and key metrics

IVBXF News
Catalyst Timeline

10 upcoming, 1 past

Phase 2Next

IBI302 8mg dose Phase 2 Est. Readout

August 2026~IBI302 8mg dose800

Estimated primary completion for IBI302 8mg dose trial (NCT07275840) in Neovascular Age-related Macular Degeneration. Topline data typically follows completion by weeks to months.

Source
Phase 3

IBI306 Phase 3 Est. Readout

September 2026~IBI306198

Estimated primary completion for IBI306 trial (NCT07473960) in Non-Familial Hypercholesterolemia and Mixed Hyperlipidemia. Topline data typically follows completion by weeks to months.

Source

8 more catalysts beyond 14 days

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Pro
Drug Pipeline

IBI306

Phase 3

Homozygous Familial Hypercholesterolemia

IBI311

Phase 3

Thyroid Eye Disease

IBI354

Phase 3

Locally Advanced Unresectable or Metastatic Solid Tumors

IBI303

Phase 3

AS

IBI301 plus CHOP

Phase 3

Diffuse, Large B-Cell, Lymphoma

Irinotecan OR Paclitaxel or Trifluridine/tipiracil( FTD/TPI)

Phase 3

Unresectable or Metastatic Gastric or Gastroesophageal Junction Adenocarcinoma

IBI308

Phase 3

Esophageal Squamous Cell Carcinoma

paclitaxel/Gemcitabine/Liposomal doxorubicin

Phase 3

Ovarian

Platinum

Phase 3

Lung Neoplasms

IBI310

Phase 3

Advanced Cervical Cancer

IBI305

Phase 3

Non-Squamous Non-Small Cell Lung Cancer

IBI343

Phase 3

Pancreatic Cancer

IBI112

Phase 3

Psoriasis

Febuxostat

Phase 3

Gout

Sintilimab

Phase 3

Esophageal Squamous Cell Carcinoma

IBI305 in Combination with Paclitaxel/Carboplatin

Phase 3

NSCLC

IBI362

Phase 3

Type 2 Diabetes

IBI310&Sintilimab

Phase 3

MSI-H

IBI306 450mg SC Q4W

Phase 3

Hypercholesterolemia

Picankibart

Phase 3

Plaque Psoriasis

IBI302

Phase 2

Diabetic Macular Oedema

dose 1 IBI302

Phase 2

Neovascular Age-related Macular Degeneration

Period 2 IBI112 dose 3

Phase 2

Ulcerative Colitis (UC)

GFH925

Phase 2

KRAS G12C

IBI311 (20 mg)

Phase 2

Thyroid Eye Disease

Low dose IBI302

Phase 2

Neovascular Age-related Macular Degeneration

IBI3003

Phase 2

Multiple Myeloma

IBI112 dose 2

Phase 2

Psoriasis

PD1

Phase 2

Relapsed/Refractory Classical Hodgkin's Lymphoma

IBI376

Phase 2

Indolent Non-hodgkin Lymphoma

IBI363

Phase 2

Melanoma

IBI334

Phase 2

Advanced Solid Tumors

IBI130

Phase 2

Solid Tumor

IBI129

Phase 2

Solid Tumor

IBI343,sintilimab,oxaliplatin,S-1

Phase 2

CLDN18.2 Positive

IBI302 8mg dose

Phase 2

Neovascular Age-related Macular Degeneration

regular treatment

Phase 2

Psoriasis

IBI343,Gemcitabine, Albumin-bound Paclitaxel

Phase 2

CLDN18.2 Positive

IBI128

Phase 2

Gout

Pemigatinib

Phase 2

Cholangiocarcinoma

IBI3014

Phase 2

Unresectable Locally Advanced or Metastatic Solid Tumors

IBI133

Phase 2

Locally Advanced Unresectable or Metastatic Solid Tumors

IBI3002

Phase 2

Atopic Dermatitis

Market-Implied Move
Regulatory Approvals

Frequently asked questions

What is in Innovent Biologics Inc/ADR's drug pipeline?

CatalystAlert tracks 43 drug candidates in Innovent Biologics Inc/ADR's (IVBXF) pipeline across Phase 3, Phase 2. Its lead program is IBI306 (Phase 3). Each drug's phase, indication and upcoming catalysts are listed on this page.

When is Innovent Biologics Inc/ADR's next FDA catalyst?

Innovent Biologics Inc/ADR's (IVBXF) next tracked catalyst is a Phase 2 expected August 30, 2026. See the catalyst timeline on this page for the full schedule of PDUFA dates, trial readouts and FDA events.

How do I track IVBXF biotech catalysts?

Add IVBXF to your CatalystAlert watchlist for alerts ahead of each catalyst, and follow Innovent Biologics Inc/ADR's live catalyst calendar, drug pipeline and clinical-trial timeline on this page — sourced from ClinicalTrials.gov, FDA and SEC filings.

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Data is aggregated from public sources (FDA, SEC, ClinicalTrials.gov). While we strive for accuracy, information may be incomplete, delayed, or contain errors. Terms apply