Developer docs
API playgroundTry for free, no card

Search company profiles

Geron

Full company profile

uuid0002u1s

Namestring
Geron
Legal namestring
Geron Corporation
Websiteurl
geron.com
Company typeenum
Public
Founded yearint
1990
Descriptiontext

Geron Corporation is a commercial-stage biopharmaceutical company headquartered in Foster City, California, founded in 1990 and publicly traded on NASDAQ under the ticker GERN. The company develops and commercializes innovative therapies for hematologic malignancies based on telomerase inhibition, a mechanism originating from Nobel Prize-winning discoveries by Elizabeth Blackburn, Carol Greider and Jack Szostak. Geron's sole approved and commercialized product is RYTELO (imetelstat), a first-in-class telomerase inhibitor oligonucleotide approved by the FDA in June 2024 and by the European Commission in March 2025 for the treatment of adults with lower-risk myelodysplastic syndromes (LR-MDS) with transfusion-dependent anemia.

The company's revenue is generated entirely from RYTELO product sales, distributed through specialty pharmacy channels and a direct field sales force targeting hematologists and oncologists across approximately 1,450 prescribing accounts in the United States, with European expansion underway. FY2025 RYTELO revenue was $183.6 million, more than doubling from $76.5 million in FY2024, and Q1 2026 revenue reached $51.8 million (+31% YoY), with FY2026 guidance of $220-240 million. The product pipeline extends imetelstat into myelofibrosis (Phase 3 IMpactMF, Phase 1 IMproveMF), AML, and high-risk MDS (Phase 2 IMpress, Phase 1/2 IMAGINE), supported by 8 company-sponsored clinical trials and more than 10 investigator-sponsored studies. The business is funded by $341 million in liquidity (including a $250M BioPharma Credit term loan facility and a prior $150M underwritten equity offering), providing approximately 2.7 years of cash runway.

Recent corporate actions include a December 2025 strategic restructuring reducing headcount by approximately one-third (from 260 to ~175), the appointment of Harout Semerjian as President and CEO in August 2025, and the installation of a largely new executive team spanning commercial, technical, legal, and corporate development functions. RYTELO's inclusion in NCCN Guidelines as a preferred second-line option for LR-MDS supports adoption, while the company's first-in-class status and dual US/EU regulatory approvals form the foundation of its competitive position. Geron operates as a single-product, multi-indication biopharmaceutical company with a concentrated asset base and an expanding geographic and clinical footprint.

Short descriptiontext

Geron Corporation is a commercial-stage biopharmaceutical company that develops and markets RYTELO (imetelstat), a first-in-class telomerase inhibitor approved in the US and EU for adults with lower-risk myelodysplastic syndromes and transfusion-dependent anemia, serving hematologists and oncologists through specialty pharmacy and direct sales channels.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
251–500
akta.pro rankint
HeadquartersFoster City, United States
HQ citystring
Foster City
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
telomerase inhibition therapy, myelodysplastic syndromes treatment, hematologic malignancy drugs, oncology biopharmaceutical products, imetelstat cancer therapy
Industry2 codes
1Rare Neurology & Neurodegenerative Disorder Therapies
CodeHLAIAIADPrimaryYes
2Genetic & Genomic Rare Disease Therapeutics
CodeHLAIAIAAPrimaryNo
NAICS code1 code
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Oncology Pharmaceuticals
Social media profiles1 record
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model1 record
1RYTELO (imetelstat) Product Sales
TypeOne Time License
Description

Commercial-stage biopharmaceutical company generating revenue from sales of its FDA and EU-approved drug RYTELO for lower-risk MDS with transfusion-dependent anemia. Revenue grew from $76.5M in 2024 to $183.6M in 2025, with Q1 2026 revenue of $51.8M showing 31% year-over-year growth. 2026 guidance: $220-240 million.

seekingalpha.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Technology or R&D, Personnel, Marketing or Sales, Supply Chain, Operations
Pricing details1 tier
1Wholesale acquisition cost information available for RYTELO
ModelOtherBilling cadenceMonthly
Notes

Wholesale Acquisition Cost Information document published on company website. Specific pricing not extracted from sources.

geron.com
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 5 records shown
1RYTELO
Description

RYTELO (imetelstat) is the company's FDA and EU-approved first-in-class telomerase inhibitor for treating adults with lower-risk myelodysplastic syndromes (LR-MDS) with transfusion-dependent anemia.

geron.com
+4 more records
Core offering1 text field

Geron is a commercial-stage biopharmaceutical company that develops and commercializes RYTELO (imetelstat), a first-in-class telomerase inhibitor approved in the U.S. and EU for treating adults with lower-risk myelodysplastic syndromes (LR-MDS) with transfusion-dependent anemia. The company also has an active clinical pipeline exploring imetelstat in additional hematologic malignancies including myelofibrosis and acute myeloid leukemia.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • 37.5% red blood cell transfusion independence rate lasting at least 8 weeks in heavily pretreated LR-MDS patients
+2 more records
Product overview1 text field

Geron is a commercial-stage biopharmaceutical company focused on developing and commercializing innovative medicines for hematologic malignancies. The company's sole approved product is RYTELO (imetelstat), a first-in-class telomerase inhibitor approved for treating adults with lower-risk MDS with transfusion-dependent anemia in both the U.S. (approved June 2024) and EU (approved March 2025). The product pipeline includes multiple clinical trials exploring imetelstat in additional indications: IMpactMF (Phase 3 in relapsed/refractory myelofibrosis), IMproveMF (Phase 1 combination with ruxolitinib in frontline myelofibrosis), IMpress (Phase 2 in AML/high-risk MDS), and IMAGINE (Phase 1/2 in relapsed/refractory AML). Geron operates as a single-product company with its commercial focus on expanding RYTELO uptake and pursuing additional regulatory approvals for the broader myelofibrosis indication.

Product and service1 record
1RYTELO (imetelstat)
CategoryOncology Pharmaceuticals
Description

RYTELO is a first-in-class telomerase inhibitor approved for the treatment of adults with lower-risk myelodysplastic syndromes (LR-MDS) with transfusion-dependent anemia. It is approved for use in both the United States (FDA, June 2024) and European Union (European Commission, March 2025) and is prescribed by hematologists and oncologists and dispensed through specialty pharmacy networks.

Scale indicator6 records

Each record includes

Type, Value, Description, Source

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

BMS markets REBLOZYL (luspatercept), the most direct approved competitor to RYTELO in lower-risk MDS, as well as fedratinib in myelofibrosis and a broad hematology/oncology portfolio. Competes with Geron across overlapping patient populations and physician call points.

TypeDirect peer
Description

Incyte markets ruxolitinib (JAKAFI), the standard of care for myelofibrosis and a key backbone in frontline MF treatment where imetelstat is being tested in combination (IMproveMF). Competes with Geron for the same heme-onc prescribers and in overlapping MF development programs.

TypeBroad incumbent
Description

GSK acquired Sierra Oncology and markets momelotinib (OMJJARA) for myelofibrosis, directly competing with imetelstat's IMpactMF indication in JAK inhibitor relapsed/refractory MF. Both companies target the same post-JAK inhibitor patient population.

TypeEmerging player
Description

Disc Medicine is a clinical-stage hematology company developing therapeutics for hematologic diseases including MDS and other anemias. Comparable in stage and indication overlap, with potential to compete for the same physician audience and addressable patient population.

TypeEmerging player
Description

Forma Therapeutics (now part of Novo Nordisk) developed etavopivat for sickle cell disease and other rare hematologic conditions. Comparable as a focused rare hematology drug developer with similar target physician audience and rare disease commercial model.

TypeBroad incumbent
Description

AbbVie acquired Pharmacyclics and markets IMBRUVICA (ibrutinib) in hematologic malignancies, with deep heme-onc commercial infrastructure and prescribers overlapping with Geron's RYTELO target audience. Represents the kind of large incumbent that could pursue assets adjacent to Geron's pipeline.

TypeEmerging player
Description

Karyopharm commercializes XPOVIO (selinexor) in multiple myeloma and is exploring hematology indications. Comparable as a small-cap hematology-focused commercial-stage biopharma with a single primary asset and similar commercialization dynamics.

TypeBroad incumbent
Description

Through the Celgene acquisition, BMS markets VIDAZA (azacitidine) and other MDS therapies, making it a historical incumbent in MDS treatment. Geron's IMpress and IMAGINE trials test imetelstat in combination or in settings where azacitidine is standard of care.

TypeBroad incumbent
Description

Takeda has a sizable hematology franchise including ADCETRIS and broader oncology infrastructure. Comparable as a major heme-onc player that overlaps with Geron's prescriber base and could pursue adjacent indications.

TypeBroad incumbent
Description

Pfizer maintains a significant hematology and oncology franchise post-Seagen acquisition, with deep heme-onc commercial reach and clinical development capacity that overlaps with Geron's customer base. Represents a potential strategic acquirer or competitor depending on indication overlap.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks7 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers1 record

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature2 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles16 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds8 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors13 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Geron

Oncology Pharmaceuticalsgeron.com

Geron Corporation is a commercial-stage biopharmaceutical company that develops and markets RYTELO (imetelstat), a first-in-class telomerase inhibitor approved in the US and EU for adults with lower-risk myelodysplastic syndromes and transfusion-dependent anemia, serving hematologists and oncologists through specialty pharmacy and direct sales channels.

What Geron does

Geron Corporation is a commercial-stage biopharmaceutical company headquartered in Foster City, California, founded in 1990 and publicly traded on NASDAQ under the ticker GERN. The company develops and commercializes innovative therapies for hematologic malignancies based on telomerase inhibition, a mechanism originating from Nobel Prize-winning discoveries by Elizabeth Blackburn, Carol Greider and Jack Szostak. Geron's sole approved and commercialized product is RYTELO (imetelstat), a first-in-class telomerase inhibitor oligonucleotide approved by the FDA in June 2024 and by the European Commission in March 2025 for the treatment of adults with lower-risk myelodysplastic syndromes (LR-MDS) with transfusion-dependent anemia.

The company's revenue is generated entirely from RYTELO product sales, distributed through specialty pharmacy channels and a direct field sales force targeting hematologists and oncologists across approximately 1,450 prescribing accounts in the United States, with European expansion underway. FY2025 RYTELO revenue was $183.6 million, more than doubling from $76.5 million in FY2024, and Q1 2026 revenue reached $51.8 million (+31% YoY), with FY2026 guidance of $220-240 million. The product pipeline extends imetelstat into myelofibrosis (Phase 3 IMpactMF, Phase 1 IMproveMF), AML, and high-risk MDS (Phase 2 IMpress, Phase 1/2 IMAGINE), supported by 8 company-sponsored clinical trials and more than 10 investigator-sponsored studies. The business is funded by $341 million in liquidity (including a $250M BioPharma Credit term loan facility and a prior $150M underwritten equity offering), providing approximately 2.7 years of cash runway.

Recent corporate actions include a December 2025 strategic restructuring reducing headcount by approximately one-third (from 260 to ~175), the appointment of Harout Semerjian as President and CEO in August 2025, and the installation of a largely new executive team spanning commercial, technical, legal, and corporate development functions. RYTELO's inclusion in NCCN Guidelines as a preferred second-line option for LR-MDS supports adoption, while the company's first-in-class status and dual US/EU regulatory approvals form the foundation of its competitive position. Geron operates as a single-product, multi-indication biopharmaceutical company with a concentrated asset base and an expanding geographic and clinical footprint.

Geron firmographics

Firmographics
Name
Geron
Legal name
Geron Corporation
Website
https://geron.com
Company type
Public
Founded year
1990
Operating status
Operating
Headcount range
251–500 employees
Short description
Geron Corporation is a commercial-stage biopharmaceutical company that develops and markets RYTELO (imetelstat), a first-in-class telomerase inhibitor approved in the US and EU for adults with lower-risk myelodysplastic syndromes and transfusion-dependent anemia, serving hematologists and oncologists through specialty pharmacy and direct sales channels.
Ownership category
akta.pro rank

Geron industry classification

Industry
Product category
Oncology Pharmaceuticals
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Rare Neurology & Neurodegenerative Disorder Therapies (HLAIAIAD)
akta.pro secondary industry
Genetic & Genomic Rare Disease Therapeutics (HLAIAIAA)

Keywords

  • Telomerase inhibition therapy
  • Myelodysplastic syndromes treatment
  • Hematologic malignancy drugs
  • Oncology biopharmaceutical products
  • Imetelstat cancer therapy

Where Geron is headquartered

Location

Headquarters

HQ city
Foster City
HQ country
United States
HQ region
North America

Offices2 records

Markets served

Geron business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Marketing or Sales, Supply Chain, Operations

Revenue model

  1. RYTELO (imetelstat) Product Sales: Commercial-stage biopharmaceutical company generating revenue from sales of its FDA and EU-approved drug RYTELO for lower-risk MDS with transfusion-dependent anemia. Revenue grew from $76.5M in 2024 to $183.6M in 2025, with Q1 2026 revenue of $51.8M showing 31% year-over-year growth. 2026 guidance: $220-240 million.

Pricing tiers

ModelBillingPrice
OtherMonthlyWholesale acquisition cost information available for RYTELO

Go-to-market motion2 records

Distribution channels3 records

Marketing channels5 records

Geron product offering

Product offering

Core offering

Geron is a commercial-stage biopharmaceutical company that develops and commercializes RYTELO (imetelstat), a first-in-class telomerase inhibitor approved in the U.S. and EU for treating adults with lower-risk myelodysplastic syndromes (LR-MDS) with transfusion-dependent anemia. The company also has an active clinical pipeline exploring imetelstat in additional hematologic malignancies including myelofibrosis and acute myeloid leukemia.

Product overview

Geron is a commercial-stage biopharmaceutical company focused on developing and commercializing innovative medicines for hematologic malignancies. The company's sole approved product is RYTELO (imetelstat), a first-in-class telomerase inhibitor approved for treating adults with lower-risk MDS with transfusion-dependent anemia in both the U.S. (approved June 2024) and EU (approved March 2025). The product pipeline includes multiple clinical trials exploring imetelstat in additional indications: IMpactMF (Phase 3 in relapsed/refractory myelofibrosis), IMproveMF (Phase 1 combination with ruxolitinib in frontline myelofibrosis), IMpress (Phase 2 in AML/high-risk MDS), and IMAGINE (Phase 1/2 in relapsed/refractory AML). Geron operates as a single-product company with its commercial focus on expanding RYTELO uptake and pursuing additional regulatory approvals for the broader myelofibrosis indication.

Differentiator

Problem solved

Functional benefit

Brands

  • RYTELO: RYTELO (imetelstat) is the company's FDA and EU-approved first-in-class telomerase inhibitor for treating adults with lower-risk myelodysplastic syndromes (LR-MDS) with transfusion-dependent anemia.
  • IMpactMF
  • IMproveMF
  • IMpress
  • IMAGINE

Products and services

  • RYTELO (imetelstat) RYTELO is a first-in-class telomerase inhibitor approved for the treatment of adults with lower-risk myelodysplastic syndromes (LR-MDS) with transfusion-dependent anemia. It is approved for use in both the United States (FDA, June 2024) and European Union (European Commission, March 2025) and is prescribed by hematologists and oncologists and dispensed through specialty pharmacy networks.

Quantifiable outcome

  • 37.5% red blood cell transfusion independence rate lasting at least 8 weeks in heavily pretreated LR-MDS patients
  • +2 more outcomes

Companies that use Geron

Customer profile

Named customers1 record

Segments3 records

Ideal customer profiles2 records

Geron technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature2 records

Geron partnerships and signals

Strategic signal

Scale indicators6 records

Recent moves7 records

Expansion highlights5 records

Geron competitors and assessment

Company assessment

Broad incumbents

  • Bristol-Myers Squibb: BMS markets REBLOZYL (luspatercept), the most direct approved competitor to RYTELO in lower-risk MDS, as well as fedratinib in myelofibrosis and a broad hematology/oncology portfolio. Competes with Geron across overlapping patient populations and physician call points.
  • GSK plc: GSK acquired Sierra Oncology and markets momelotinib (OMJJARA) for myelofibrosis, directly competing with imetelstat's IMpactMF indication in JAK inhibitor relapsed/refractory MF. Both companies target the same post-JAK inhibitor patient population.
  • AbbVie: AbbVie acquired Pharmacyclics and markets IMBRUVICA (ibrutinib) in hematologic malignancies, with deep heme-onc commercial infrastructure and prescribers overlapping with Geron's RYTELO target audience. Represents the kind of large incumbent that could pursue assets adjacent to Geron's pipeline.
  • Bristol-Myers Squibb (Celgene legacy): Through the Celgene acquisition, BMS markets VIDAZA (azacitidine) and other MDS therapies, making it a historical incumbent in MDS treatment. Geron's IMpress and IMAGINE trials test imetelstat in combination or in settings where azacitidine is standard of care.
  • Takeda Pharmaceutical: Takeda has a sizable hematology franchise including ADCETRIS and broader oncology infrastructure. Comparable as a major heme-onc player that overlaps with Geron's prescriber base and could pursue adjacent indications.
  • Pfizer: Pfizer maintains a significant hematology and oncology franchise post-Seagen acquisition, with deep heme-onc commercial reach and clinical development capacity that overlaps with Geron's customer base. Represents a potential strategic acquirer or competitor depending on indication overlap.

Direct peers

  • Incyte Corporation: Incyte markets ruxolitinib (JAKAFI), the standard of care for myelofibrosis and a key backbone in frontline MF treatment where imetelstat is being tested in combination (IMproveMF). Competes with Geron for the same heme-onc prescribers and in overlapping MF development programs.

Emerging players

  • Disc Medicine: Disc Medicine is a clinical-stage hematology company developing therapeutics for hematologic diseases including MDS and other anemias. Comparable in stage and indication overlap, with potential to compete for the same physician audience and addressable patient population.
  • Forma Therapeutics: Forma Therapeutics (now part of Novo Nordisk) developed etavopivat for sickle cell disease and other rare hematologic conditions. Comparable as a focused rare hematology drug developer with similar target physician audience and rare disease commercial model.
  • Karyopharm Therapeutics: Karyopharm commercializes XPOVIO (selinexor) in multiple myeloma and is exploring hematology indications. Comparable as a small-cap hematology-focused commercial-stage biopharma with a single primary asset and similar commercialization dynamics.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks7 records

Key highlights7 records

Customer concentration

Geron social profiles

Digital presence

Geron financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Geron leadership team

Management profile

Number of profiles

Profiles16 records

Geron funding detail

Funding detail

Funding overview

Funding rounds8 records

Investors13 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Geron M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Geron

What does Geron do?

Geron is a commercial-stage biopharmaceutical company that develops and commercializes RYTELO (imetelstat), a first-in-class telomerase inhibitor approved in the U.S. and EU for treating adults with lower-risk myelodysplastic syndromes (LR-MDS) with transfusion-dependent anemia. The company also has an active clinical pipeline exploring imetelstat in additional hematologic malignancies including myelofibrosis and acute myeloid leukemia.

Is Geron a public or private company?

Geron is a public company. It is classified as public and is currently operating.

When was Geron founded?

Geron was founded in 1990. It employs 251 to 500 people.

Where is Geron based?

Geron is headquartered in Foster City, United States, in the North America region.

How does Geron make money?

One revenue line is on record: RYTELO (imetelstat) Product Sales.

Who are Geron's main competitors?

Broad incumbents on record are Bristol-Myers Squibb, GSK plc, AbbVie, Bristol-Myers Squibb (Celgene legacy), Takeda Pharmaceutical and Pfizer. Incyte Corporation is listed as a direct peer. Emerging players are Disc Medicine, Forma Therapeutics and Karyopharm Therapeutics.

Does Geron have an API?

No public API is recorded for Geron.

What industry is Geron in?

Geron's product category is Oncology Pharmaceuticals. Its primary akta.pro industry code is HLAIAIAD, Rare Neurology & Neurodegenerative Disorder Therapies, with a secondary code of HLAIAIAA, Genetic & Genomic Rare Disease Therapeutics. Its NAICS code is 541714 and its SIC code is 2834.

Unlock the full company data

50 free credits on sign-up, no credit card required.

Contact sales
Live signals
PR NewswireDid Geron Corporation Insiders Breach their Fiduciary Duties to Shareholders?Halper Sadeh LLC is investigating whether Geron Corporation officers and directors breached fiduciary duties to shareholders. The firm invites long-term Geron shareholders to seek corporate governance reforms, return of funds, or other relief on a contingent fee basis.PR NewswireGeron Investigation Initiated: Kahn Swick & Foti, LLC Investigates the Officers and Directors of Geron Corporation - GERNKahn Swick & Foti, LLC announced an investigation into Geron Corporation's officers and directors. The probe follows a securities class action alleging failure to disclose material information about Rytelo's revenue flatlining due to seasonality, competition, and monitoring requirements. The firm seeks to determine if fiduciary duties were breached.BioSpaceGeron Corporation Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4) - September 18, 2026Geron Corporation granted stock options to purchase 821,250 shares to nine newly hired employees, effective September 17, 2026. The options have an exercise price of $1.32 per share, a ten-year term, and vest over four years. The awards were made under Nasdaq Listing Rule 5635(c)(4) and the company's 2018 Inducement Award Plan.Stock TitanGeron Grants 821,250-Share Inducement OptionsGeron Corporation granted 821,250 inducement stock options to nine new hires at a $1.32 exercise price, vesting over four years. The options, granted under Nasdaq Listing Rule 5635(c)(4), have a ten-year term with 12.5% vesting on the six-month anniversary and the remainder over 42 months.Ticker ReportGeron Eyes High End of 2026 RYTELO Revenue Guidance as Community Adoption ExpandsGeron executives said the company expects 2026 RYTELO net revenue of $220–$240 million, now targeting the midpoint to high end. The company reported $57.5 million in net revenue for the latest quarter, its highest since launch, and is shifting commercial focus to community practices. Geron plans to provide an ex-U.S. strategy before year-end.FinancialContent Business PageGeron Investigation Initiated: Kahn Swick & Foti, LLC Investigates the Officers and Directors of Geron Corporation - GERNKahn Swick & Foti, LLC announced an investigation into Geron Corporation's officers and directors. The probe follows Q4 2024 results showing Rytelo growth flattened and an ongoing securities class action. The firm seeks to determine if fiduciary duties were breached.MorningstarGeron Investigation Initiated: Kahn Swick & Foti, LLC Investigates the Officers and Directors of Geron Corporation - GERNKahn Swick & Foti, LLC has initiated an investigation into Geron Corporation's officers and directors. The investigation follows a securities class action alleging failure to disclose material information, after Geron's Rytelo revenue growth flattened in Q4 2024. The firm is seeking to determine if fiduciary duties were breached.AInvestGeron Tracks RYTELO to the High End of Guidance While Its Stock Sits Near the LowGeron's RYTELO drug generated $57.5 million in Q2 net revenue, up 11% from Q1, with H1 2026 revenue of $109.3 million. The company guides full-year 2026 RYTELO revenue to $220-240 million, requiring roughly $131 million in H2. The stock trades near $1.35 despite the company tracking to the high end of guidance.MarketBeatGeron Sees RYTELO Revenue Near High End of 2026 Guidance as Community Use ExpandsGeron expects full-year RYTELO net revenue to reach the mid-to-high end of its $230–240 million guidance, driven by expanded community use in lower-risk MDS. CEO Harout Semerjian said Q2 revenue was $57.5 million, up 24% year-over-year, and the company is shifting focus to second-line treatment and European strategy.AInvestGeron’s Lone Bull Fails to Stop Capital FlightGeron's stock fell 0.66% amid negative fund flows and bearish technical signals, despite a lone Strong Buy rating from Needham. The company shows a 90% gross margin but a -18.59% net profit margin, with all investor classes exiting. Traders are advised to wait for a confirmed reversal before buying.