PRXL on NASDAQ

PAREXEL

Logo: PAREXEL International Corporation, Public domain, via Wikimedia Commons4

Clinical trials management company

Parexel is an American contract research organization. It conducts clinical trials on behalf of its pharmaceutical and biotechnology clients to expedite drug development and clinical trial progress. Parexel was founded in 1982 by Josef von Rickenbach and organic chemist Anne B. Sayigh initially to advise Japanese and German firms on how to navigate the US Food and Drug Administration (FDA) drug approval process.2 Its shares trade on NASDAQ under the symbol PRXL.1 Wikipedia text CC BY-SA 4.0

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Last updated Oct 21, 2026.

Overview

1982Founded1

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  • TickerPRXL on NASDAQ1
  • Industrypharmaceutical industry1
  • HeadquartersWaltham1
  • Websitewww.parexel.com
  • Legal formDomestic Business Corporation3
  • LEI549300GCZVUYB6P2OA173
  • StatusActive3
  • LEI statusIssued and current3
  • Registered addressC/O PAREXEL INTERNATIONAL, 02466 Newton, United States3
  • Registered withCorporations Division (Secretary of the Commonwealth's Office), 0427762693

Parexel is an American contract research organization. It conducts clinical trials on behalf of its pharmaceutical and biotechnology clients to expedite drug development and clinical trial progress.2

Corporate structure

PAREXEL sits at the top of its group. 3 entities, 3 countries on record. Switch between the flow chart and the network, and select any entity to see its details.

Built from parent and subsidiary links from GLEIF, the Global Legal Entity Identifier Foundation (CC0); subsidiaries, stakes and holdings from Wikidata (CC0). Each entity in the chart links to its source.

The story

Parexel was founded in 1982 by chemist Anne B. Sayigh and businessperson Josef von Rickenbach in Cambridge, Massachusetts. Its name derived from the 16th century Swiss scientist, "Paracelsus", who is credited with starting the field of chemistry.

Initially, Parexel was focused on helping pharmaceutical businesses in Japan and Germany to obtain approval for their candidate drugs by the US FDA. Parexel also published a newsletter on FDA regulatory news called the U.S. Regulatory Reporter, which was the foundation of its medical marketing division.

In 1984, new legislation made it easier to produce generic drugs, leading to a rapid expansion of the market for contract research. Parexel started providing its own contract clinical research services in 1986, growing to $14.75 million in annual revenues in 1990. In the 1990s, Parexel opened new offices in California, North Carolina, Japan, Italy, and Australia. By 2018, Parexel had some 18,900 employees with operations in 100 countries.

Parexel went public on NASDAQ in 1995. It used the funding to make a series of acquisitions, including six consulting companies, two medical marketing businesses, and three European businesses in 1998. By 2018, Parexel had completed more than 40 mergers and acquisitions.

In September 2017, private equity firm Pamplona Capital Management bought Parexel for $5 billion, taking it off the public market. By this time, Parexel had more than $2 billion in annual revenues. In 2021, Parexel was acquired again for $8.5 billion by two private equity firms, EQT Private Equity and Goldman Sachs Asset Management.

In 2026, Parexel acquired Vitrana, an AI-powered pharmacovigilance platform provider, to expand its patient safety technology capabilities.

From Wikipedia’s article on Parexel, shared under CC BY-SA 4.0.5

Products and brands

With a global workforce of about 21,000 in 2025, Parexel provides clinical research support to its clients over the range of Phase I to IV clinical trials in various therapeutic categories, including neuroscience, general medicine, oncology, and infectious diseases, among others. Examples of services provided include management of clinical trial subjects and trial investigators, regulatory approval, outsourcing, market access strategies, medical communications, and drug safety assessment.

In 2024, Parexel established a collaboration with Palantir Technologies, a software company using artificial intelligence for data management solutions in clinical trials.

From Wikipedia’s article on Parexel, shared under CC BY-SA 4.0.5

Subsidiaries and ownership

Subsidiaries

From Wikidata.1

Timeline

  1. 1982Founded Founded1

Calendar

Drug trials and FDA: coming up

  1. Nov 2, 2026Phase 3 trial readout expected Phase 3 trial of Anifrolumab in Cutaneous Lupus Erythematosus, run by AstraZeneca: primary completion expected Nov 2, 2026 (ClinicalTrials.gov NCT06015737).6
  2. Dec 1, 2026Phase 2 trial readout expected Phase 2 trial of PRL3-zumab in Solid Tumor, run by Intra-IMMUSG Pte Ltd: primary completion expected Dec 1, 2026 (ClinicalTrials.gov NCT04452955).7
  3. Dec 23, 2026Phase 3 trial readout expected Phase 3 trial of Benralizumab in Asthma, run by AstraZeneca: primary completion expected Dec 23, 2026 (ClinicalTrials.gov NCT05692180).8
  4. Jan 6, 2027Phase 3 trial readout expected Phase 3 trial of PLENVU® and Sodium picosulfate in Bowel Cleansing Prior to Clinical Procedures, run by Norgine: primary completion expected Jan 6, 2027 (ClinicalTrials.gov NCT07218523).9
  5. Feb 22, 2027Phase 3 trial readout expected Phase 3 trial of Osimertinib in Cancer, run by AstraZeneca: primary completion expected Feb 22, 2027 (ClinicalTrials.gov NCT05629234).10
  6. Oct 13, 2027Phase 3 trial readout expected Phase 3 trial of BDA MDI and AS MDI in Asthma, run by AstraZeneca: primary completion expected Oct 13, 2027 (ClinicalTrials.gov NCT06307665).11

Drug trials and FDA: recently

  1. Jan 20, 2026Phase 3 trial completed Phase 3 trial of Tivozanib and Nivolumab in Renal Cell Carcinoma, run by AVEO Pharmaceuticals, Inc.: primary completion Jan 20, 2026, no results posted yet (ClinicalTrials.gov NCT04987203).12
  2. Nov 4, 2025Phase 3 trial completed Phase 3 trial of Acalabrutinib in Chronic Lymphocytic Leukemia, run by AstraZeneca: primary completion Nov 4, 2025, results posted Sep 1, 2026 (ClinicalTrials.gov NCT04008706).13
  3. Oct 28, 2024Phase 3 trial completed Phase 3 trial of Osimertinib (AZD9291) pemetrexed cisplatin or carboplatin in Non-small Cell Lung Cancer, run by AstraZeneca: primary completion Oct 28, 2024, results posted Jan 13, 2026 (ClinicalTrials.gov NCT04765059).14

Upcoming dates from Nasdaq's calendar; past results from the company's 8-K filings (Item 2.02). Trials from ClinicalTrials.gov, as the sponsor registered them (expected dates are the sponsor's own and often move); approvals and advisory committee meetings from the FDA. The FDA does not publish its decision (PDUFA) dates. The full markets calendar

Sources

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