> Trialight public data. Index of pages: https://trialight.com/llms.txt
> Web page: https://trialight.com/data/company/arcus-biosciences-inc-5db51387-2105-4a17-8261-60c8f8ffb028
> Record changed: 2026-10-13

# Arcus Biosciences, Inc.

Headquarters country

United States

Source: [www.sec.gov](https://www.sec.gov/cgi-bin/browse-edgar?action=getcompany&CIK=0001724521)

Registry sponsor category

Industry

Source: [clinicaltrials.gov](https://clinicaltrials.gov/)

## Names and classification

**Other names**

- Arcus Biosciences, Inc.

**Company name**

Arcus Biosciences, Inc.

**Organisation type**

Industry

**Registered legal name**

Arcus Biosciences, Inc.

Source: [www.sec.gov](https://www.sec.gov/cgi-bin/browse-edgar?action=getcompany&CIK=0001724521)

**US industry code (SIC)**

Pharmaceutical preparations

Source: [www.sec.gov](https://www.sec.gov/cgi-bin/browse-edgar?action=getcompany&CIK=0001724521)

**Registry sponsor category**

Industry

Source: [clinicaltrials.gov](https://clinicaltrials.gov/)

**Website**

https://arcusbio.com/

Source: [www.wikidata.org](https://www.wikidata.org/wiki/Q113503877)

## Location and listing

**Headquarters country**

United States

Source: [www.sec.gov](https://www.sec.gov/cgi-bin/browse-edgar?action=getcompany&CIK=0001724521)

**Publicly traded (proxy)**

Yes

**Listing at source**

Listed

## Identifiers

**SEC filer number (CIK)**

0001724521

Source: [www.sec.gov](https://www.sec.gov/cgi-bin/browse-edgar?action=getcompany&CIK=0001724521)

**Wikidata ID**

Q113503877

Source: [www.wikidata.org](https://www.wikidata.org/wiki/Q113503877)

## Related records

### Trials (56)

- A Bioequivalence Study Between Two Casdatifan Tablet Strengths and Food Effect Study of Casdatifan in Healthy Adult Participants
- [A Clinical Trial of a New Combination Treatment, Domvanalimab and Zimberelimab, Plus Chemotherapy, for People With an Upper Gastrointestinal Tract Cancer That Cannot be Removed With Surgery That Has Spread to Other Parts of the Body](https://trialight.com/data/trial/a-clinical-trial-of-a-new-combination-treatment-domvanalimab-855f2af6-2909-4db2-a114-5887eeab4af4.md)
- A Drug-Drug Interaction Study to Evaluate the Effect of Itraconazole on the Pharmacokinetic Profile of Etrumadenant in Healthy Adult Participants
- A Global Study to Assess the Effects of Durvalumab + Domvanalimab Following Concurrent Chemoradiation in Participants With Stage III Unresectable NSCLC
- [A Phase 1 Study of AB521 Monotherapy and Combination Therapies in Renal Cell Carcinoma and Other Solid Tumors](https://trialight.com/data/trial/a-phase-1-study-of-ab521-monotherapy-and-combination-e1b2f8d0-943b-4fb4-a208-30e7ab9efff0.md)
- A Phase I-II Study to Test the Safety and Efficacy of PD1 (AB122) and Adenosine Receptor (AB928) Antagonists With Chemotherapy After Short-Course Radiation for Rectal Cancer.
- A Relative Bioavailability Study and Food Effect Study of AB521 in Healthy Adult Volunteers
- [A Safety and Efficacy Study of Treatment Combinations With and Without Chemotherapy in Adult Participants With Advanced Upper Gastrointestinal Tract Malignancies](https://trialight.com/data/trial/a-safety-and-efficacy-study-of-treatment-combinations-with-3f4b398e-ad9f-4d15-84a8-5055bc61e278.md)
- A Study Investigating the Safety, Absorption, and Elimination of Radioactively Labeled Etrumadenant, a New Compound in the Treatment of Cancer
- A Study of AB801 Monotherapy and Combination Therapy in Participants With Advanced Malignancies
- A Study of Concurrent Chemoradiation in Combination With or Without PD1 Inhibitor AB122 Adenosine 2a Receptor / Adenosine 2b Receptor Inhibitor AB928 Therapies in Locally Advanced Head and Neck Cancers
- A Study to Assess the Safety, Pharmacokinetics, and Pharmacodynamics of AB801 in Healthy Volunteers
- A Study to Evaluate AB308 in Combination With AB122 in Participants With Advanced Malignancies
- A Study to Evaluate Immunotherapy Combinations in Participants With Gastrointestinal Malignancies
- A Study to Evaluate Immunotherapy Combinations in Participants With Lung Cancer
- A Study to Evaluate Pharmacokinetics (PK) of Etrumadenant Tablet and Capsule Formulations in Healthy Adult Participants
- A Study to Evaluate Safety/Tolerability of Immunotherapy Combinations in Participants With Triple-Negative Breast Cancer or Gynecologic Malignancies
- A Study to Evaluate the Safety and Tolerability of AB154 in Participants With Advanced Malignancies
- A Study to Evaluate the Safety and Tolerability of AB680 in Participants With Gastrointestinal Malignancies
- A Study to Evaluate the Safety and Tolerability of Immunotherapy Combinations in Participants With Advanced Malignancies

---

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