Agios Pharmaceuticals, Inc. (AGIO)

NASDAQ: AGIO · Real-Time Price · USD
40.55
-0.68 (-1.65%)
Jul 13, 2026, 4:00 PM EDT - Market closed
Market Cap2.41B +27.3%
Revenue (ttm)66.05M +78.3%
Net Income-422.60M
EPS-7.25
Shares Out 59.47M
PE Ration/a
Forward PEn/a
Dividendn/a
Ex-Dividend Daten/a
Volume713,874
Open40.67
Previous Close41.23
Day's Range39.43 - 41.10
52-Week Range22.24 - 46.00
Beta0.54
AnalystsBuy
Price Target42.63 (+5.13%)
Earnings DateJul 30, 2026

About AGIO

Agios Pharmaceuticals, Inc., a biopharmaceutical company, discovers and develops medicines in the field of cellular metabolism in the United States. Its lead product includes PYRUKYND (mitapivat), an activator of wild-type and mutant pyruvate kinase (PK), enzymes used for the treatment of hemolytic anemias in adults with PK deficiency. The company’s PYRUKYND product is also used for the treatment of sickle cell disease that is in phase 3 clinical trial; for the treatment of PK deficiency in pediatric patients; and AQVESME for the treatment of a... [Read more]

Industry Biotechnology
Sector Healthcare
IPO Date Jul 24, 2013
Employees 540
Stock Exchange NASDAQ
Ticker Symbol AGIO
Full Company Profile

Financial Performance

Financial Statements

Analyst Summary

According to 10 analysts, the average rating for AGIO stock is "Buy." The 12-month stock price target is $42.63, which is an increase of 5.13% from the latest price.

Price Target
$42.63
(5.13% upside)
Analyst Consensus: Buy
Stock Forecasts

News

Agios Pharmaceuticals rises 13.5%

Agios Pharmaceuticals (AGIO) is up 13.5%, or $5.04 to $42.43.

6 days ago - TheFly

Leerink sees Priority Review designation as positive sign for Agios’ mitapivat

Leerink notes that Agios Pharmaceuticals (AGIO) announced the FDA granted Priority Review for the sNDA for mitapivat in sickle cell disease with a PDUFA date of 11/1/26 suggesting imminent approval.

6 days ago - TheFly

H.C. Wainwright sees FDA Priority Review as positive signal for Agios’ mitapivat

H.C. Wainwright analyst Emily Bodnar notes that Agios Pharmaceuticals (AGIO) announced that the FDA accepted its sNDA for mitapivat, in sickle cell disease under the accelerated approval pathway with ...

6 days ago - TheFly

Agios Pharmaceuticals rises 12.9%

Agios Pharmaceuticals (AGIO) is up 12.9%, or $4.81 to $42.20.

6 days ago - TheFly

Agios Pharmaceuticals price target raised to $46 from $40 at BofA

BofA raised the firm’s price target on Agios Pharmaceuticals (AGIO) to $46 from $40 and keeps a Buy rating on the shares. Company-compiled consensus of $26.9M appears achievable based on…

6 days ago - TheFly

Agios Pharmaceuticals price target raised to $41 from $36 at Truist

Truist raised the firm’s price target on Agios Pharmaceuticals (AGIO) to $41 from $36 and keeps a Buy rating on the shares as part of a broader research note updating…

6 days ago - TheFly

Agios Pharmaceuticals price target raised to $32 from $28 at RBC Capital

RBC Capital raised the firm’s price target on Agios Pharmaceuticals (AGIO) to $32 from $28 and keeps a Sector Perform rating on the shares as part of a broader research…

6 days ago - TheFly

Agios Pharmaceuticals granted priority review for mitapivat sNDA

Agios Pharmaceuticals (AGIO) announced that the FDA has accepted its supplemental new drug application for mitapivat, an oral pyruvate kinase activator, in sickle cell disease with a priority review. ...

6 days ago - TheFly

U.S. FDA Grants Priority Review to Agios' sNDA for Mitapivat in Sickle Cell Disease

FDA's PDUFA goal date is November 1, 2026 If approved, mitapivat is positioned to become the first oral PK activator for patients with sickle cell disease CAMBRIDGE, Mass., July 07, 2026 (GLOBE NEWSWI...

6 days ago - GlobeNewsWire

Agios to Host Second Quarter 2026 Financial Results Conference Call and Webcast on July 30 at 8:00 a.m. ET

CAMBRIDGE, Mass., June 29, 2026 (GLOBE NEWSWIRE) -- Agios Pharmaceuticals, Inc. (Nasdaq: AGIO), a commercial-stage biopharmaceutical company focused on delivering innovative medicines for patients wit...

14 days ago - GlobeNewsWire

Agios Pharmaceuticals price target raised to $54 from $50 at H.C. Wainwright

H.C. Wainwright raised the firm’s price target on Agios Pharmaceuticals (AGIO) to $54 from $50 and keeps a Buy rating on the shares. The company over the weekend presented numerous…

4 weeks ago - TheFly

Agios Pharmaceuticals presented results from Phase 3 trial of mitapivat

Agios Pharmaceuticals (AGIO) presented detailed results from the 52-week double-blind period of the global RISE UP Phase 3 trial of mitapivat. These efficacy and safety results, which include new tran...

4 weeks ago - TheFly

Agios Showcases RISE UP Phase 3 Results at EHA 2026 Plenary Session Reinforcing Strong Anti-Hemolytic Profile of Mitapivat in Sickle Cell Disease

Mitapivat demonstrated statistically significant improvement in hemoglobin response compared with placebo, with rapid onset and durable effects New analyses showed patients in mitapivat arm had clinic...

4 weeks ago - GlobeNewsWire

Agios Pharmaceuticals Transcript: EHA 2026

The conference highlighted robust clinical data for mitapivat in thalassemia and sickle cell disease, including durable hemoglobin improvements, reduced transfusion needs, and a favorable safety profile. Strategic expansion into new indications and strong commercial execution position the company for growth in rare hematology.

4 weeks ago - Transcripts

Agios Pharmaceuticals Slides: FY 2026

Agios Pharmaceuticals has posted slides in relation to its FY 2026 quarterly earnings report, which was published on June 13, 2026.

4 weeks ago - Filings

Agios Pharmaceuticals price target lowered to $31 from $36 at JPMorgan

JPMorgan lowered the firm’s price target on Agios Pharmaceuticals (AGIO) to $31 from $36 and keeps a Neutral rating on the shares. The past few months have been active for…

4 weeks ago - TheFly

Agios Pharmaceuticals Transcript: Status update

Announced a global license for cevidoplenib, a next-gen SYK inhibitor for ITP, with a capital-efficient deal structure and strong commercial synergies. Phase II data show durable efficacy and favorable safety, supporting phase III initiation in 2028.

6 weeks ago - Transcripts

Agios Pharmaceuticals Slides: Status update

Agios Pharmaceuticals has posted slides in relation to its latest quarterly earnings report, which was published on June 1, 2026.

6 weeks ago - Filings

Agios Pharmaceuticals Press release: Status update

Agios Pharmaceuticals issued a press release on June 1, 2026, disclosing material business information to investors.

6 weeks ago - Filings

Agios Pharmaceuticals enters license pact with Oscotec to develop cevidoplenib

Agios Pharmaceuticals (AGIO) announced an agreement with Oscotec, headquartered in South Korea, to license the exclusive global rights to cevidoplenib, an oral spleen tyrosine kinase inhibitor. Agios ...

6 weeks ago - TheFly

Agios Enters Exclusive Global License Agreement with Oscotec to Develop and Commercialize Next-Generation SYK Inhibitor Cevidoplenib

Agios obtains exclusive global rights to novel, late-stage, next-generation, oral SYK inhibitor Agreement diversifies Agios' rare hematology portfolio with expansion into immune thrombocytopenia, unlo...

6 weeks ago - GlobeNewsWire

Agios Pharmaceuticals price target lowered to $40 from $41 at BofA

BofA lowered the firm’s price target on Agios Pharmaceuticals (AGIO) to $40 from $41 and keeps a Buy rating on the shares after the company announced tebapivat will not advance…

6 weeks ago - TheFly

Agios scraps blood cancer drug program after study miss

Agios Pharmaceuticals said on Friday ​it will stop developing its ‌experimental drug for a form of blood cancer after a ​mid-stage trial failed to ​show enough benefit.

6 weeks ago - Reuters

Agios will not advance tebapivat in lower-risk myelodysplastic syndromes

Agios Pharmaceuticals (AGIO) announced that it will not advance tebapivat, a next-generation oral pyruvate kinase activator, in lower-risk myelodysplastic syndromes. This decision follows results from...

6 weeks ago - TheFly

Agios Provides Update on Phase 2b Trial of Tebapivat in Lower-Risk Myelodysplastic Syndromes

Results did not meet predefined threshold to support further development in LR-MDS Tebapivat was well tolerated, with no new safety signals observed CAMBRIDGE, Mass., May 29, 2026 (GLOBE NEWSWIRE) -- ...

6 weeks ago - GlobeNewsWire