Syndax Pharmaceuticals, Inc. (SNDX)

NASDAQ: SNDX · Real-Time Price · USD
13.08
+0.23 (1.79%)
At close: Dec 20, 2024, 4:00 PM
12.52
-0.56 (-4.29%)
After-hours: Dec 20, 2024, 6:38 PM EST
1.79%
Market Cap 1.12B
Revenue (ttm) 16.00M
Net Income (ttm) -297.06M
Shares Out 85.36M
EPS (ttm) -3.62
PE Ratio n/a
Forward PE n/a
Dividend n/a
Ex-Dividend Date n/a
Volume 4,322,787
Open 12.78
Previous Close 12.85
Day's Range 12.76 - 13.15
52-Week Range 12.76 - 25.34
Beta 0.84
Analysts Strong Buy
Price Target 37.64 (+187.77%)
Earnings Date Nov 5, 2024

About SNDX

Syndax Pharmaceuticals, Inc., a clinical-stage biopharmaceutical company, develops therapies for the treatment of cancer. Its lead product candidates are revumenib, a potent, selective, small molecule inhibitor of the menin-MLL binding interaction for the treatment of KMT2A rearranged, acute leukemias, and solid tumor; and SNDX-6352 or axatilimab, a monoclonal antibody that blocks the colony stimulating factor 1, or CSF-1 receptor for the treatment of patients with chronic graft versus host disease (cGVHD) and idiopathic pulmonary fibrosis (IPF... [Read more]

Industry Biotechnology
Sector Healthcare
IPO Date Mar 3, 2016
Employees 184
Stock Exchange NASDAQ
Ticker Symbol SNDX
Full Company Profile

Financial Performance

Financial Statements

Analyst Forecast

According to 11 analysts, the average rating for SNDX stock is "Strong Buy." The 12-month stock price forecast is $37.64, which is an increase of 187.77% from the latest price.

Price Target
$37.64
(187.77% upside)
Analyst Consensus: Strong Buy
Stock Forecasts

News

Syndax Announces Additional Positive Data for Revuforj® (revumenib) from AUGMENT-101 Trial in Relapsed or Refractory mNPM1 AML and BEAT AML Frontline Combination Trial

– Subgroup analyses from Ph 2 protocol-defined R/R mNPM1 AML efficacy population (N=64) show responses across all major subgroups, including heavily pretreated patients – – 26% CR+CRh (20/77) and 48% ...

12 days ago - PRNewsWire

Syndax Presents Positive Revuforj® (revumenib) Data in Acute Leukemias from Multiple Trials, Including the SAVE Combination and AUGMENT-101 Trials, at 66th ASH Annual Meeting

–        82% ORR (27 of 33 pts) and 48% CR/CRh (16 of 33 pts) in SAVE trial studying revumenib in combination with venetoclax and decitabine/cedazuridine in R/R AML – –        64% ORR (62 of 97 pts) a...

13 days ago - PRNewsWire

Syndax Pharmaceuticals Reports Inducement Grants Under NASDAQ Listing Rule 5635(c)(4)

WALTHAM, Mass. , Dec. 3, 2024 /PRNewswire/ -- Syndax Pharmaceuticals (Nasdaq: SNDX), a commercial-stage biopharmaceutical company developing an innovative pipeline of cancer therapies, today announced...

17 days ago - PRNewsWire

Syndax Announces Participation at the Citi 2024 Global Healthcare Conference

WALTHAM, Mass. , Nov. 27, 2024 /PRNewswire/ -- Syndax Pharmaceuticals (Nasdaq: SNDX), a commercial stage biopharmaceutical company developing an innovative pipeline of cancer therapies, today announce...

24 days ago - PRNewsWire

US FDA approves Syndax's blood cancer drug

The U.S. Food and Drug Administration on Friday approved Syndax Pharmaceuticals' drug for the treatment of adult and pediatric patients with a type of blood cancer, sending the company's shares up 3% ...

5 weeks ago - Reuters

Syndax Announces FDA Approval of Revuforj® (revumenib), the First and Only Menin Inhibitor to Treat Adult and Pediatric Patients with Relapsed or Refractory Acute Leukemia with a KMT2A Translocation

– Approval based on positive data from the AUGMENT-101 clinical trial, in which Revuforj delivered robust and durable rates of remission in R/R acute leukemia patients with a KMT2A translocation – – S...

5 weeks ago - PRNewsWire

Syndax: Fall On NPM1m AML Data Of Revumenib Creates Buy Opportunity

Primary endpoint of pivotal phase 2 study met with statistical significance in using Revumenib for the treatment of relapsed/refractory mNPM1 AML patients; sNDA expected 1st half 2025. PDUFA action da...

5 weeks ago - Seeking Alpha

Syndax Announces Positive Pivotal Topline Results from Relapsed or Refractory mNPM1 AML Cohort in AUGMENT-101 Trial of Revumenib

–      Primary endpoint met with CR/CRh rate of 23% in pivotal Ph 2 cohort of R/R mNPM1 AML patients (p-value = 0.0014) – –      47% (30/64) ORR in a heavily pre-treated population, including 75% with...

5 weeks ago - PRNewsWire

Syndax Pharmaceuticals, Inc. (SNDX) Q3 2024 Earnings Call Transcript

Syndax Pharmaceuticals, Inc. (NASDAQ:SNDX) Q3 2024 Earnings Conference Call November 5, 2024 4:30 PM ET Company Participants Sharon Klahre - Head, Investor Relations Michael Metzger - Chief Executive...

6 weeks ago - Seeking Alpha

Syndax Reports Third Quarter 2024 Financial Results and Provides Business Update

–  New revumenib and Niktimvo ™  clinical data will be highlighted at 66th ASH Annual Meeting – – mNPM1 AML topline data from AUGMENT-101 expected in 4Q24; potential sNDA filing in 1H25 – – Revumenib ...

6 weeks ago - PRNewsWire

Syndax to Host ASH Investor Event in Person and via Webcast on December 9, 2024

WALTHAM, Mass. , Nov. 5, 2024 /PRNewswire/ -- Syndax Pharmaceuticals (Nasdaq: SNDX), a commercial-stage biopharmaceutical company developing an innovative pipeline of cancer therapies, today announced...

6 weeks ago - PRNewsWire

Syndax Announces Revumenib Abstracts to Be Presented at the 66th ASH Annual Meeting

– New monotherapy and combination data in acute leukemia further highlight revumenib's compelling clinical profile –  – 64% ORR (62/97) in expanded dataset of patients with R/R KMT2Ar acute leukemia i...

6 weeks ago - PRNewsWire

Syndax Announces New Data from Secondary Analysis of the Pivotal AGAVE-201 Trial of Niktimvo™ (axatilimab-csfr) in Chronic Graft-Versus-Host Disease to Be Presented at 66th ASH Annual Meeting

– Rapid responses and symptom improvement observed in inflammatory and fibrotic manifestations of chronic GVHD in heavily pretreated patients – WALTHAM, Mass. , Nov. 5, 2024 /PRNewswire/ -- Syndax Pha...

6 weeks ago - PRNewsWire

Syndax Pharmaceuticals and Royalty Pharma Enter into $350 Million Royalty Funding Agreement for Niktimvo™

Proceeds expected to support the upcoming planned launches and fund the continued development of Niktimvo and revumenib Expected to fund Company through profitability; proforma cash approaching $800 m...

Other symbols: RPRX
6 weeks ago - PRNewsWire

Syndax Announces Participation in November Investor Conferences

WALTHAM, Mass. , Nov. 1, 2024 /PRNewswire/ -- Syndax Pharmaceuticals (Nasdaq: SNDX), a commercial-stage biopharmaceutical company developing an innovative pipeline of cancer therapies, today announced...

7 weeks ago - PRNewsWire

Syndax to Announce Third Quarter 2024 Financial Results and Host Conference Call and Webcast on November 5, 2024

WALTHAM, Mass. , Oct. 29, 2024 /PRNewswire/ -- Syndax Pharmaceuticals (Nasdaq: SNDX), a commercial-stage biopharmaceutical company developing an innovative pipeline of cancer therapies, today announce...

7 weeks ago - PRNewsWire

Incyte and Syndax Announce New England Journal of Medicine Publication of Data from Pivotal AGAVE-201 Trial of Niktimvo™ (axatilimab-csfr) in Chronic Graft-Versus-Host Disease

– Trial met its primary endpoint across all dose cohorts with 74% of patients at the 0.3 mg/kg every 2 weeks dose achieving a complete or partial response within the first six months of treatment – – ...

Other symbols: INCY
3 months ago - PRNewsWire

Foundation Medicine Partners with Syndax to Develop a Companion Diagnostic in Hematology and Support Efforts to Pursue Regulatory Approval for an Assay Based on the FoundationOne®Heme Platform

BOSTON--(BUSINESS WIRE)--Foundation Medicine partners with Syndax to develop a companion diagnostic to identify acute myeloid leukemia patients harboring an NPM1 mutation.

3 months ago - Business Wire

Syndax Announces Publication in the Journal of Clinical Oncology of Data from the Pivotal AUGMENT-101 Trial of Revumenib in Relapsed/Refractory KMT2Ar Acute Leukemia

– Pivotal AUGMENT-101 trial met its primary endpoint at interim analysis of patients with KMT2Ar AML and ALL (p-value = 0.0036) – – NDA filing for revumenib in R/R KMT2Ar acute leukemia is being revie...

4 months ago - PRNewsWire

Syndax Pharmaceuticals, Inc. (SNDX) Q2 2024 Earnings Call Transcript

Syndax Pharmaceuticals, Inc. (SNDX) Q2 2024 Earnings Call Transcript

5 months ago - Seeking Alpha

Syndax Reports Second Quarter 2024 Financial Results and Provides Clinical and Business Update

–  Axatilimab BLA in refractory chronic GVHD is under Priority Review; PDUFA action date of August 28, 2024 – – Revumenib NDA in R/R KMT2Ar acute leukemia is being reviewed under RTOR; PDUFA action da...

5 months ago - PRNewsWire

FDA Delays Decision on Syndax Leukemia Drug; Stock Sinks

Shares of Syndax Pharmaceuticals (SNDX) plunged in intraday trading Monday after the biopharmaceutical company reported that the Food and Drug Administration (FDA) delayed a decision on approving its ...

5 months ago - Investopedia

Syndax Announces PDUFA Action Date Extension for Revumenib NDA for Relapsed or Refractory KMT2Ar Acute Leukemia

– New PDUFA action date of December 26, 2024 allows FDA additional time to complete their review –  WALTHAM, Mass. , July 29, 2024 /PRNewswire/ -- Syndax Pharmaceuticals (Nasdaq: SNDX), a clinical sta...

5 months ago - PRNewsWire

Syndax to Announce Second Quarter 2024 Financial Results and Host Conference Call and Webcast on August 1, 2024

WALTHAM, Mass. , July 25, 2024 /PRNewswire/ -- Syndax Pharmaceuticals (Nasdaq: SNDX), a clinical-stage biopharmaceutical company developing an innovative pipeline of cancer therapies, today announced ...

5 months ago - PRNewsWire

Syndax Presents Updated Positive Data from BEAT AML and AUGMENT-102 Phase 1/2 Combination Trials of Revumenib in Patients with Acute Leukemias at EHA 2024 Congress

- Data continue to support revumenib's potential to enhance current standard of care agents - - 96% CRc (23 of 24 pts) observed in BEAT AML trial exploring revumenib in combination with venetoclax/aza...

6 months ago - PRNewsWire