Fundraising Fox

OncoResponse

Houston, US · Founded 2015 · Delaware corporation · 7 known investors

oncoresponseinc.com

Clinical-stage immuno-oncology company developing antibodies derived from the immune systems of 'Elite' cancer responders.

Also known as OncoResponse, Inc.

Biotech

Founders & leadership

AB
Alice BexonExecutive
CJ
Clifford J. StocksExecutive
KD
Kamal D. PuriExecutive
CR
Chris RussellExecutive
RH
Russ HawkinsonExecutive

Board

SGSteven Gillis
Steven GillisinBoard directorManaging Director at ARCH Venture Partners
CG
Carol GallagherBoard director
JMJohn McKearn
John McKearnin𝕏Board directorSenior Advisor at RiverVest Venture Partners, focused on early-stage biotech
WHWende Hutton
Wende Huttonin𝕏Board directorGeneral Partner at Canaan Partners
RDRoberto De Ponti
Roberto De PontiinBoard directorSenior Advisor at Claris Ventures
APAndrew Perlman
Andrew PerlmaninBoard directorManaging Partner at GreatPoint Ventures
SM
Sean McCarthyBoard director

Investors · 7

Reported raises · per SEC filings

Form D private placements

$109M disclosed across 5 rounds · 2015–2025

$6MraisedMay 2025 · 9 investors · Biotechnology
Rule 506(b)
Officers, directors & promoters on the filing
  • Sean A. McCarthyDirector
  • Roberto De PontiDirector
  • Alice BexonExecutive Officer
  • Steven GillisDirector
  • Clifford J. StocksDirector, Executive Officer
  • Kamal D. PuriExecutive Officer
  • Carol GallagherDirector
  • John McKearnDirector
  • Chris RussellExecutive Officer
  • Wende HuttonDirector
Amount sold
$6M
First sale
Apr 2025
Incorporated
Corporation, Delaware
Federal exemptions
06b
Full filing on SEC EDGAR ↗
$13.9MraisedMay 2023 · 13 investors · Biotechnology
Rule 506(b)
Officers, directors & promoters on the filing
  • Roberto DePontiDirector
  • Ted KoutouzisDirector
  • Steven GillisDirector
  • Kamal D. PuriExecutive Officer
  • Sean McCarthyDirector
  • Robert LechleiderExecutive Officer
  • Wende HuttonDirector
  • Christopher A. RussellExecutive Officer
  • Clifford J. StocksExecutive Officer, Director
  • John McKearnDirector
Offering amount
$40M
Amount sold
$13.9M
Proceeds to insiders
$4.8M
First sale
May 2023
Incorporated
Corporation, Delaware
Federal exemptions
06b
Full filing on SEC EDGAR ↗
$40.6MraisedMar 2021 · 14 investors · Biotechnology
Rule 506(b)
Officers, directors & promoters on the filing
  • Clifford StocksExecutive Officer, Director
  • Roberto DePontiDirector
  • Steven GillisDirector
  • Wende HuttonDirector
  • Ted KoutouzisDirector
  • John McKearnDirector
  • Patrick Joseph HojloDirector
  • Daguang WangDirector
  • Bob LechleiderExecutive Officer
  • Kamal PuriExecutive Officer
Offering amount
$60M
Amount sold
$40.6M
Proceeds to insiders
$1.4M
First sale
Mar 2021
Incorporated
Corporation, Delaware
Federal exemptions
06b
Full filing on SEC EDGAR ↗
$19MraisedSep 2018 · 12 investors · Biotechnology
Rule 506(b)
Officers, directors & promoters on the filing
  • Clifford StocksExecutive Officer, Director
  • Steven GillisDirector
  • John McKearnDirector
  • Andrew PerlmanDirector
  • Roberto DePontiDirector
  • Wende HuttonDirector
  • Nathan JorgensenDirector
Offering amount
$40M
Amount sold
$19M
Proceeds to insiders
$1.2M
First sale
Aug 2018
Incorporated
Corporation, Delaware, 2015
Federal exemptions
06b
Full filing on SEC EDGAR ↗
$29.5MraisedMar 2017 · 12 investors · Biotechnology
Rule 506(b)
Officers, directors & promoters on the filing
  • Clifford StocksExecutive Officer, Director
  • Roberto De PontiDirector
  • Andrew PerlmanDirector
  • Russ HawkinsonExecutive Officer
  • Steve GillisDirector
  • Wende HuttonDirector
  • Alan GinsbergDirector
Offering amount
$34M
Amount sold
$29.5M
First sale
Sep 2015
Incorporated
Corporation, Delaware, 2015
Federal exemptions
06b
Full filing on SEC EDGAR ↗

Source: SEC EDGAR Form D. Amounts as filed; amended filings shown once at their latest values.

Company profile

researched Aug 2026

OncoResponse is a clinical-stage immuno-oncology biotechnology company that discovers and develops therapeutic antibodies against cancer targets, with a focus on the tumor microenvironment. Its central approach is to interrogate the immune systems of so-called Elite Cancer Responders — patients who responded exceptionally well to cancer immunotherapy — using a proprietary B-cell discovery platform to identify fully human monoclonal antibodies. Much of the pipeline targets immunosuppressive myeloid cells and tumor-associated macrophages, with the stated goal of relieving macrophage-mediated immune suppression and converting immunologically 'cold' tumors into 'hot' ones.

The lead clinical candidate, OR2805 (zovostotug), is a fully human anti-CD163 monoclonal antibody derived from an Elite Responder to checkpoint inhibitor therapy; it is being evaluated in an open-label, multicenter, first-in-human Phase 1/2 dose-escalation and expansion study (NCT05094804, started September 2021) as monotherapy and in combination with other anticancer agents in advanced solid tumors, and has entered cohort expansion in multiple indications. A second program, OR502, is an anti-LILRB2 antibody intended to rescue innate and adaptive immune responses from LILRB2-mediated suppression; it is in a Phase 1/2 study alone and in combination with cemiplimab (NCT06090266, started October 2023). Additional preclinical programs include a LILRB1 x LILRB2 bispecific antibody in hematologic neoplasms, anti-Siglec-15 antibodies, and ONCR-201, an anti-EMP2 fully human monoclonal antibody acquired with Paganini Biopharma in 2017 and originally developed for female malignancies. The company holds issued US patents covering immunomodulatory antibodies (US-11034770-B2, US-11634501-B2, US-12195549-B2) and human CD163 antibodies (US-11827715-B2).

Founding story

The company was launched by Theraclone Sciences together with The University of Texas MD Anderson Cancer Center as an immuno-oncology antibody discovery startup capitalized with an initial $9.5 million, built around the idea of targeting 'super-responders' to immunotherapy. Clifford J. Stocks is described as founder and CEO.

Business model

OncoResponse operates as a private, venture- and grant-funded therapeutics developer: it discovers antibody drug candidates in-house, advances them through preclinical and early clinical development, and pursues strategic alliances, collaborations, and licensing or co-development agreements. Manufacturing activities such as cell line development, process development, and cGMP Phase I/II clinical supply are outsourced to CDMO partners.

No product revenue is described in the sources; the company is financed through venture equity, debt (a $50 million Oxford Finance credit facility is referenced), state grant funding from CPRIT, and partnering/licensing arrangements.

Traction

Two active Phase 1/2 trials are listed as recruiting; OR2805 has advanced into cohort expansion across multiple cancer indications, and OR502 began dosing in October 2023. The company has generated preclinical and clinical data presented at AACR and other scientific meetings, holds at least four issued US patents, and maintains a strategic alliance with MD Anderson Cancer Center. Reported headcount is in the 10-50 range.

Latest developments

In May 2023 the company announced a $13 million CPRIT grant and a concurrent $14 million financing from existing investors led by RiverVest Venture Partners. OR502 began its Phase 1/2 trial in October 2023. A $6 million venture round appeared in an initial SEC filing dated May 6, 2025, and company leadership presented at the J.P. Morgan 43rd Annual Healthcare Conference and AACR 2025.

Full profile — market position, technology, go-to-market, geography, history, risks & controversies

Market position

The company positions itself in immuno-oncology as a developer of myeloid- and macrophage-directed antibodies intended to complement or improve upon checkpoint inhibitor therapy, describing OR502 as a best-in-class anti-LILRB2 antibody. It has been profiled by trade press as an emerging biotech to watch in novel immuno-oncology concepts.

Differentiation rests on sourcing antibodies from the B cells of patients who responded exceptionally well to checkpoint inhibitor therapy, rather than from conventional target-first discovery, and on a pipeline concentrated on immunosuppressive macrophage biology (CD163, LILRB2, Siglec-15, EMP2) in the tumor microenvironment.

Technology

The core technology is a proprietary B-cell discovery platform that screens human immune repertoires from Elite Responders to checkpoint inhibitor therapy to identify fully human monoclonal antibodies. Supporting capabilities include antibody humanization and engineering for macrophage targets, in vitro macrophage functional assays, in vivo tumor models, translational biomarker assays embedded in clinical trials, and cell line/process development for biologics executed with CDMO partners.

Go-to-market

Development-stage go-to-market centers on clinical trial execution at multicenter sites, presentation of data at scientific and investor conferences (AACR, ASCO, SITC, J.P. Morgan Healthcare Conference, Needham, Piper Sandler, Berenberg, RBC, SVB), academic collaboration for biospecimen and translational access, and business development aimed at alliances and licensing.

Ultimately patients with advanced solid tumors and hematologic malignancies treated by oncologists; near-term counterparties are pharmaceutical and biotechnology partners, academic cancer centers, and investors.

Geography

Offices and addresses cited include 609 Main Street, Suite 4200, Houston, Texas, and Seattle, Washington (one database lists Washington State as the company location). Clinical studies are multicenter.

History

Following its launch by Theraclone and MD Anderson, OncoResponse reported $29.5 million in funding, then closed a $40 million Series B (reported variously as $40M and $40.6M) that shifted it from discovery into development. In November 2017 it acquired Paganini Biopharma, adding the anti-EMP2 antibody ONCR-201. It entered the clinic with OR2805 in September 2021, secured a $50 million credit facility with Oxford Finance, and in May 2023 was awarded a $13 million CPRIT grant alongside a $14 million insider-led financing. OR502 entered clinical study in October 2023, and a further $6 million raise was disclosed in an SEC filing in May 2025. Corporate address information appears in both Seattle/Washington and Houston, Texas.

Risks & controversies

No controversies are reported in the sources. Standard early-stage biotechnology risks are implied by the profile: all programs are preclinical or in Phase 1/2, no products are approved, and the company depends on continued equity, debt, and grant financing as well as outsourced CDMO manufacturing and its MD Anderson alliance.

Compiled by commissioned research from 8 cited public sources — announcements, filings, and press listed under research sources below.

Key figures

latest reported
Active clinical trialsMar 20262 trials
Employee count (range)Mar 202610-50
Highest development phaseMar 2026Phase 1/2 (OR2805/zovostotug and OR502)
Issued US patents listedJan 20254 patents

Company-reported or press-reported figures, each dated to when it was claimed — not independently audited.

Timeline · 7

launches, deals, and filings
May 2025
$6 million venture round disclosed in initial SEC filing

$6M source ↗

Oct 2023
Phase 1/2 trial of OR502 (anti-LILRB2) begins

NCT06090266, an open-label multicenter first-in-human dose-escalation and expansion study of OR502 alone and in combination with cemiplimab in advanced solid tumors; sponsored by OncoResponse and listed as recruiting.

source ↗

May 2023
$14 million financing from existing investors led by RiverVest Venture Partners

$14M source ↗

May 2023
Awarded $13 million grant from CPRIT

The Cancer Prevention and Research Institute of Texas awarded OncoResponse a $13 million grant to support advancement of OR502, an anti-LILRB2 antibody, toward IND and clinical studies.

$13M source ↗

May 2023
Broad strategic alliance with MD Anderson Cancer Center

OncoResponse deploys its proprietary B-cell discovery platform under a broad strategic alliance with MD Anderson Cancer Center to identify antibodies targeting immune cells in the tumor microenvironment.

source ↗

Sep 2021
First-in-human Phase 1/2 trial of OR2805 (anti-CD163) begins

NCT05094804, an open-label multicenter dose-escalation and expansion study of OR2805 as monotherapy and in combination with anticancer agents in advanced solid tumors; sponsored by OncoResponse and listed as recruiting.

source ↗

Nov 2017
OncoResponse closes acquisition of Paganini Biopharma, adding anti-EMP2 antibody ONCR-201

OncoResponse acquired all assets of Paganini Biopharma, including ONCR-201, a fully human anti-epithelial membrane protein 2 (EMP2) monoclonal antibody originating from UCLA under a license from the UCLA Technology Development Group. Financial terms were not disclosed. Paganini co-founder Madhuri Wadehra became a consultant to OncoResponse.

source ↗

Dated company events from announcements, filings, and press; legal rows summarize public dockets and regulator releases.

Legal entities · 1

corporate structure
OncoResponseDelaware

In the news

Research sources · 8

primary sources listed

8 public sources were cited for this profile; the first-party ones are listed here.

Frequently asked questions

What does OncoResponse do?
Clinical-stage immuno-oncology company developing antibodies derived from the immune systems of 'Elite' cancer responders.
Who are OncoResponse's investors?
OncoResponse's investors include 3B Future Health Fund, Canaan Partners, GreatPoint Ventures, RiverVest Venture Partners, ARCH Venture Partners, Qatar Investment Authority, Yonjin Venture LLC.
How much funding has OncoResponse raised?
OncoResponse has disclosed $109M raised across 5 rounds.
Where is OncoResponse headquartered?
OncoResponse is headquartered in Houston, US.