Last10K.com

Cytomx Therapeutics, Inc. (CTMX) SEC Filing 10-Q Quarterly report for the period ending Sunday, March 31, 2019

Cytomx Therapeutics, Inc.

CIK: 1501989 Ticker: CTMX

Exhibit 99.1


CytomX Therapeutics Announces Full-Year 2018 Financial Results

-Company to Host a Conference Call Today, February 27, 2019, at 5:00 p.m. EST / 2:00 p.m. PST-

SOUTH SAN FRANCISCO, CA., February 27, 2019 -- CytomX Therapeutics, Inc. (Nasdaq: CTMX), a clinical-stage oncology-focused biopharmaceutical company pioneering a novel class of investigational antibody therapeutics based on its Probody™ therapeutic technology platform, today reported full-year 2018 financial results. As part of its 2019 Research and Development Day held yesterday in New York, CytomX provided an operational update on the company.

As of December 31, 2018, CytomX had cash, cash equivalents and short-term investments of $436.1 million, sufficient capital to fund its operating expenses and capital requirement into 2021.

“Over the last year, we have generated meaningful clinical proof of concept data for the Probody platform across both of our lead, wholly-owned programs,” said Sean McCarthy, D.Phil., president, chief executive officer and chairman of CytomX Therapeutics.  “As we showed at our inaugural Research and Development Day yesterday, our PD-L1 Probody therapeutic, CX-072, is active across a wide range of tumors and has a potentially differentiated safety profile as monotherapy and in combination.  CX-2009, our first-in-class CD166 Probody Drug Conjugate, is well tolerated and has demonstrated anti-tumor activity across multiple tumor types. In 2019, we will continue to explore the full potential of these innovative product candidates as we maintain our intense focus on discovery, development and ultimate commercialization of a new generation of differentiated cancer therapeutics.”

2018 Business Highlights and Recent Developments

PROCLAIM-CX-072 (PD-L1 Probody Therapeutic) Clinical Program

 

CX-072 is a Probody therapeutic targeting PD-L1, a clinically- and commercially-validated anti-cancer target.

 

Enrollment began in January 2017 in PROCLAIM-CX-072, a Phase 1/2 clinical trial evaluating CX-072 as monotherapy and in combination with YERVOY® (ipilimumab) or Zelboraf® (vemurafenib) in patients with cancer.

 

Enrollment is complete with follow-up continuing in the monotherapy dose escalation arm evaluating CX-072 in patients with advanced unresectable solid tumors or lymphomas (Part A) and in the monotherapy dose escalation arm in patients with PD-L1-positive tumors (Part A2).

 

Enrollment and follow-up are ongoing in the monotherapy expansion cohorts of CX-072 at 10 mg/kg in multiple indications (Part D).

 

Data from Parts A, A2 and D was presented most recently at CytomX’s 2019 Research and Development Day.

 

Additional data from Part D is expected in 2019.

1

 


The following information was filed by Cytomx Therapeutics, Inc. (CTMX) on Wednesday, February 27, 2019 as an 8K 2.02 statement, which is an earnings press release pertaining to results of operations and financial condition. It may be helpful to assess the quality of management by comparing the information in the press release to the information in the accompanying 10-Q Quarterly Report statement of earnings and operation as management may choose to highlight particular information in the press release.

View differences made from one quarter to another to evaluate Cytomx Therapeutics, Inc.'s financial trajectory

Compare SEC Filings Year-over-Year (YoY) and Quarter-over-Quarter (QoQ)
Sample 10-K Year-over-Year (YoY) Comparison

Compare this 10-Q Quarterly Report to its predecessor by reading our highlights to see what text and tables were  removed  ,   added    and   changed   by Cytomx Therapeutics, Inc..

Continue

Assess how Cytomx Therapeutics, Inc.'s management team is paid from their Annual Proxy

Definitive Proxy Statement (Form DEF 14A)
Screenshot example of actual Proxy Statement

Cytomx Therapeutics, Inc.'s Definitive Proxy Statement (Form DEF 14A) filed after their 2019 10-K Annual Report includes:

  • Voting Procedures
  • Board Members
  • Executive Team
  • Salaries, Bonuses, Perks
  • Peers / Competitors

Continue

SEC Filing Tools

Rating

Learn More
Bullish Bearish Neutral
Filter Sentiment:
All
Positive
Negative
Filter Category:
All
Financial
M & A
Revenue
Other
Filter Subcategory:
All
Expense
Cash Flow
Product
Geography
Income
Other
Inside Cytomx Therapeutics, Inc.'s 10-Q Quarterly Report:

Financial Statements, Disclosures and Schedules

Inside this 10-Q Quarterly Report

Document And Entity Information
Condensed Balance Sheets
Condensed Balance Sheets (Parenthetical)
Condensed Statements Of Cash Flows
Condensed Statements Of Operations And Comprehensive Loss
Statements Of Stockholders' Equity
Accrued Liabilities
Accrued Liabilities (Tables)
Accrued Liabilities - Summary Of Accrued Liabilities (Details)
Basis Of Presentation And Summary Of Significant Accounting Policies
Basis Of Presentation And Summary Of Significant Accounting Policies (Policies)
Basis Of Presentation And Summary Of Significant Accounting Policies (Tables)
Basis Of Presentation And Summary Of Significant Accounting Policies - Additional Information (Details)
Basis Of Presentation And Summary Of Significant Accounting Policies - Summary Of Reconciliation Of Cash, Cash Equivalents, And Restricted Cash (Details)
Description Of The Business
Fair Value Measurements And Short-Term Investments
Fair Value Measurements And Short-Term Investments (Tables)
Fair Value Measurements And Short-Term Investments - Additional Information (Details)
Fair Value Measurements And Short-Term Investments - Schedule Of Short-Term Investments Subject To Fair Value Measurements On A Recurring Basis (Details)
Income Tax Expense
Income Tax Expense - Additional Information (Details)
Leases
Leases (Tables)
Leases - Additional Information (Details)
Leases - Summary Of Supplemental Information Related To Leases (Details)
Net Loss Per Share
Net Loss Per Share (Tables)
Net Loss Per Share - Summary Of Potentially Dilutive Securities Excluded From Computation Of Diluted Net Loss Per Share (Details)
Research And Collaboration Agreements
Research And Collaboration Agreements (Tables)
Research And Collaboration Agreements - Abbvie Ireland Unlimited Company - Additional Information (Details 1)
Research And Collaboration Agreements - Abbvie Ireland Unlimited Company - Additional Information (Details)
Research And Collaboration Agreements - Amgen, Inc - Additional Information (Details)
Research And Collaboration Agreements - Bristol-Myers Squibb Company - Additional Information (Details)
Research And Collaboration Agreements - Contract Liabilities - Additional Information (Details)
Research And Collaboration Agreements - Immunogen, Inc - Additional Information (Details)
Research And Collaboration Agreements - Pfizer Inc - Additional Information (Details)
Research And Collaboration Agreements - Schedule Of Revenue By Collaboration Partners (Details)
Research And Collaboration Agreements - Summary Of Contract Liabilities (Details)
Stock-Based Compensation
Stock-Based Compensation (Tables)
Stock-Based Compensation - Schedule Of Activities Under Company's Stock Option Plans (Details)
Stock-Based Compensation - Total Stock-Based Compensation Recognized (Details)
Subsequent Event
Subsequent Event - Additional Information (Details)
Ucsb License Agreement
Ucsb License Agreement - Additional Information (Details)
Ticker: CTMX
CIK: 1501989
Form Type: 10-Q Quarterly Report
Accession Number: 0001564590-19-017968
Submitted to the SEC: Thu May 09 2019 12:06:51 PM EST
Accepted by the SEC: Thu May 09 2019
Period: Sunday, March 31, 2019
Industry: Pharmaceutical Preparations

External Resources:
Stock Quote
Social Media
SEC.gov

Bookmark the Permalink:
https://last10k.com/sec-filings/ctmx/0001564590-19-017968.htm