Ambrx Provides Update On APEX-01, an On-Going Phase 1 / 2 Dose Escalation Study Evaluating ARX517, a Proprietary PSMA-Targeting ADC, in Metastatic Castration-Resistant Prostate Cancer

Rhea-AI Summary

Ambrx Biopharma, Inc. (AMAM) announced positive clinical results for its anti-PSMA antibody drug conjugate ARX517 in the APEX-01 trial for metastatic castration-resistant prostate cancer. Cohort 9 showed no dose limiting toxicities or serious adverse events, with two patients experiencing rapid PSA reduction after one dose. Cohort 8 is fully enrolled, and the recommended phase 2 dose is expected by early next year.

Positive

• Positive clinical results for ARX517 in Cohort 9 with no DLTs or SAEs
• Two patients in Cohort 9 experienced rapid PSA reduction after one dose of ARX517
• Cohort 8 is fully enrolled

Negative

• None.

Cohort 9

• Following completion of the 21-day observation period at 3.4 mg/kg (Cohort 9), no dose limiting toxicities (DLTs) or serious adverse events (SAEs) were observed
• Two patients in Cohort 9 experienced rapid PSA reduction at three weeks post-treatment following the first ARX517 dose

Cohort 8

• The cohort (2.88 mg/kg) is now fully enrolled with 20 patients
  

Recommended phase 2 dose expected by early next year

SAN DIEGO, Nov. 28, 2023 (GLOBE NEWSWIRE) -- Ambrx Biopharma, Inc., or Ambrx (NASDAQ: AMAM), today announced a clinical update regarding its proprietary anti-PSMA antibody drug conjugate (ADC) ARX517 in the ongoing APEX-01 Phase 1 / 2 dose escalation and dose expansion clinical trial in metastatic castration-resistant prostate cancer (mCRPC).

Following the completion of the 21-day DLT observation period from APEX-01 dose escalation Cohort 9 (3.4 mg/kg), no DLTs or SAEs were observed. Two of the three patients in Cohort 9 had a rapid PSA reduction of 91% and 33% at the first PSA assessment at three weeks post-treatment and following only one dose of ARX517. A PSA decrease was not reported in the third patient because the patient had non-PSA secreting mCRPC. On Monday November 27, the safety monitoring committee (SMC) voted to dose escalate to 4.5 mg/kg (Cohort 10) as well as expand patients at the 3.4 mg/kg dose (Cohort 9). All expansion cohorts, Cohort 4 (1.4 mg/kg at n=23), Cohort 6 (2.0 mg/kg at n=23), and Cohort 8 (2.88 mg/kg at n=20) are now fully enrolled.

“We continue to observe no DLTs or SAEs at the highest ARX517 dose tested. We believe this is a direct result of the stability of conjugation supported by PK data presented at ESMO last month. While we are opportunely positioned to explore higher doses, we have already observed significant PSA50 decline and long duration on treatment at 2.0 mg/kg,” said Sandra Aung, Ph.D., Chief Clinical Officer of Ambrx. “The high interest in our PSMA-targeting ADC and pace of enrollment in the APEX-01 study has been outstanding and based on this we are anticipating to reach a recommended phase 2 dose by early next year.”

About ARX517

ARX517 is an investigational antibody-drug conjugate composed of a humanized anti-PSMA mAb linked to AS269, an Ambrx proprietary potent microtubule inhibitor. ARX517 is designed to target the prostate-specific membrane antigen (PSMA). PSMA is highly expressed in metastatic castration-resistant prostate cancer (mCRPC) and has been validated as a therapeutic target.

In preclinical studies, the cancer cell killing payload of ARX517, pAF-AS269, is highly cytotoxic when delivered by a mAb into cancer cells. ARX517’s site-specific linkage, stable conjugation chemistry, and non-cleavable linker result in an ADC with a homogenous drug-antibody-ratio, mAb-like biophysical properties, and exceptional stability. Therefore, Ambrx believes ARX517 can promote highly specific tumor cell killing with minimal off-target toxicity.

ARX517 has the potential to be a first- and best-in-class anti-PSMA ADC addressing the high unmet medical need in mCRPC.

About APEX-01

Ambrx is currently investigating ARX517 in the APEX-01 (NCT04662580) first-in-human Phase 1 / 2, multicenter, dose escalation and dose expansion clinical study to evaluate the safety, pharmacokinetics, and preliminary anti-tumor activity of ARX517 in adult subjects and is currently enrolling patients with advanced prostate cancer (mCRPC) whose tumors have progressed following at least two FDA approved treatments for prostate cancer, including at least one second-generation androgen receptor pathway inhibitor, and have met one of the following three criteria: PSA progression defined by a minimum of two rising PSA values or radiographic progression by RECIST v 1.1 or disease progression by the presence of new bone lesions.

About Ambrx Biopharma, Inc.

Ambrx is a clinical-stage biopharmaceutical company using an expanded genetic code technology platform to discover and develop next-generation antibody drug conjugates (ADCs) and other engineered therapies to modulate the immune system. Ambrx is advancing a focused portfolio of clinical and preclinical programs designed to optimize efficacy and safety in multiple cancer indications, including ARX517, its proprietary ADC targeting the prostate-specific membrane antigen (PSMA) and ARX788, its proprietary ADC targeting HER2. In addition, Ambrx has preclinical and clinical collaborations with multiple partners on drug candidates generated using Ambrx technology. Ambrx was spun out of The Scripps Research Institute in 2003 and has several other product candidates utilizing ADCs and other aspects of Ambrx’s protein engineering technology. For more information, please visit www.ambrx.com. Ambrx routinely posts information that may be important to investors on its website.

Forward-Looking Statements

This press release includes certain “forward-looking statements” intended to qualify for the “safe harbor” from liability established by the Private Securities Litigation Reform Act of 1995, as amended. Forward-looking statements may be identified by the words “intend,” “plan,” and similar expressions, are based on Ambrx’s current expectations, and are subject to inherent uncertainties, risks and assumptions that are difficult to predict. Factors that could cause actual results to differ include, but are not limited to, those risks and uncertainties associated with: Ambrx’s ability to execute on its strategy, including with respect to the timing of its R&D efforts, initiation of clinical trials and other anticipated milestones; the development and marketing approval of novel therapeutics, including potential delays in clinical trials and regulatory submissions and the fact that future clinical trial results/data may not be consistent with interim, initial or preliminary results/data or results/data from prior preclinical studies or clinical trials; Ambrx’s ability to fund operations as anticipated; and the additional risks and uncertainties set forth more fully under the caption “Risk Factors” in Ambrx’s Quarterly Report on Form 10-Q filed with the SEC on November 13, 2023, and elsewhere in Ambrx’s reports filed with the SEC. Forward-looking statements contained in this press release are made as of this date, and Ambrx undertakes no duty to publicly update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as may be required under applicable law.

Contacts

INVESTORS
Mike Moyer
LifeSci Advisors
617-308-4306
mmoyer@lifesciadvisors.com

MEDIA
Karissa Cross, Ph.D.
LifeSci Communications
615-651-4622
media@ambrx.com 

Source: Ambrx Biopharma, Inc.

FAQ

What is the company name and ticker symbol of the biopharmaceutical company that announced positive clinical results for ARX517 in the APEX-01 trial for metastatic castration-resistant prostate cancer?

Ambrx Biopharma, Inc. (AMAM) announced the positive clinical results.

What were the results of Cohort 9 in the APEX-01 trial for ARX517?

Cohort 9 showed no dose limiting toxicities or serious adverse events, with two patients experiencing rapid PSA reduction after one dose of ARX517.

What is the status of Cohort 8 in the APEX-01 trial for ARX517?

Cohort 8 is fully enrolled.

When is the recommended phase 2 dose expected for ARX517?

The recommended phase 2 dose is expected by early next year.