Summary

Study QXL138AM-001 is a Phase 1a/1b study to investigate the safety, pharmacokinetics,
and preliminary activity of QXL138AM in subjects with locally advanced un-resectable
and/or metastatic solid tumors and multiple myeloma. The study is an open-label,
multicenter, first in human study to be conducted in two major parts which are further
organized into two sub-parts. Part A Dose Escalation is a modified 3+3 with the first two
cohorts consisting of one subject each based on the low clinical starting dose. Dose
escalation in solid tumors (Part A1) will be followed by dose finding in multiple myeloma
(Part A2). Part B consists of dose expansion in solid tumors (Part B1) and multiple
myeloma (Part B2) using the recommended dose for expansion from Part A

Objectives

This is an open-label, multicenter, first in human (FIH) Phase 1a/1b study of QXL138AM in
participants with locally advanced unresectable and/or metastatic solid tumors and
multiple myeloma. This study will be conducted in two parts (A and B) and each part has
two sub-parts for tumor type (1 and 2).

Part A1 - Dose Escalation in Solid Tumors The following solid tumor types will initially
be enrolled in this part: ovarian, pancreatic, urothelial, renal, hepatocellular,
gastrointestinal, lung, prostate, and breast cancer.

Dose escalation will use a standard 3+3 design, where 3 to 6 participants with advanced
solid tumors will be enrolled sequentially into each cohort/dose level with the exception
of Cohort 1 and 2. For Cohorts 1 and 2, given the very low starting dose, only one
participant is planned for each level unless a participant experiences a Grade 2 or
higher adverse event not clearly and incontrovertibly related to disease progression or
an extraneous factor. If such a Grade 2 or higher event occurs in Cohort 1 or 2, dose
escalation will switch to a standard 3+3 design. Dose escalation will continue until the
MTD or RDE is determined in participants with solid tumors, referred to as the RDE-ST. At
this point, the two solid tumor types for dose expansion will be selected for Part B1 and
may begin at the RDE-ST.

The proposed dose levels are defined in the table below. Cohort No. of Participants Dose
Level (Q2W) (mg/kg)

1. 1-6 0.001

2. 1-6 0.003

3. 3-6 0.01

4. 3-6 0.03

5. 3-6 0.1

6. 3-6 0.3

7. 3-6 1

8. 3-6 2

9. 3-6 4 Infusions will be administered via syringe pump or IV bag (depending on the
dose) and administered over a 30-60-minute (± 10 minutes) duration.

Part A2 - Dose Escalation in Multiple Myeloma Dose escalation in multiple myeloma will
commence when the RDE-ST for solid tumors has been identified, or if there are signs of
anti-tumor activity in Part A1 as determined by the Sponsor.

Dose escalation will use a standard 3+3 design, where 3 to 6 participants with multiple
myeloma will be enrolled sequentially into dose escalation cohorts starting at one dose
level below the RDE-ST determined from solid tumor dose escalation (RDE-ST-1).
Alternatively, if signs of anti-tumor activity in Part A1 are observed, the Sponsor may
elect to initiate dose escalation in multiple myeloma at one dose level below the highest
dose already deemed safe in Part A1. If two of the first six participants in the first
multiple myeloma cohort experience a DLT, then the dose will be further reduced by one
level (RDE-ST-2). Once the RDE for multiple myeloma patients is determined, it will be
referred to as the RDE-MM and dose expansion may begin in patients with multiple myeloma
at this dose.

Part B1: Dose Expansion in Solid Tumors When the RDE-ST has been identified by the SRC
from Part A1, the study may continue to Part B1 dose expansion to further explore the
safety and anti-tumor activity of QXL138AM in solid tumors. Dose expansion will enroll
two cohorts of 20 participants each in two solid tumor indications identified from Part
A1. In each cohort, patients will be randomized 1:1 to receive the RDE-ST dose or 1 dose
lower. The Sponsor may opt to enroll additional participants up to a maximum of 40 in
each cohort if signs of anti-tumor activity are observed.

Part B2: Dose Expansion in Multiple Myeloma When the RDE-MM in multiple myeloma has been
identified by the SRC from Part A2, the study may continue to Part B2 dose expansion to
further explore the safety and anti-tumor activity of QXL138AM in patients with multiple
myeloma. Up to 20 participants will be treated at the RDE-MM identified in Part A2.
Patients will be randomized 1:1 to receive the RDE-MM dose or 1 dose lower.

Eligibility

1. Participants with Solid Tumors
2. Histopathologically confirmed diagnosis of an advanced, unresectable, or metastatic solid tumor (ovarian, pancreatic, urothelial, renal, hepatocellular, gastrointestinal (GI), lung, prostate, and breast cancer).
3. Have progressed despite standard therapies, or for whom conventional therapy is not effective or tolerable, as judged by the Investigator. Patients must have no available therapeutic options known to confer clinical benefit for their tumor type.
4. Participants with Multiple Myeloma
5. Have progressed despite standard therapies, or for whom conventional therapy is not effective or tolerable, as judged by the Investigator.
6. Patients must have failed at least 3 prior therapies for myeloma and should have had prior exposure to a proteosome inhibitor, an IMiD, and an anti-CD38-directed therapy.
7. Male or female participants =18 years of age at the time of informed consent 3. An Eastern Cooperative Oncology Group (ECOG) performance status scale of 0, 1, or 2 at Screening 4. Must have at least 1 measurable lesion by RECIST version 1.1 (solid tumors only), or evaluable disease by IMWG Uniform Response Criteria (multiple myeloma only) 5. Adequate organ function and bone marrow reserve 6. Adequate cardiac function as estimated by left ventricular ejection fraction 7. Female participants of child-bearing potential must:
8. Have a negative serum pregnancy test at screening and a negative pregnancy test at Week 1 Day 1 prior to first dose of QXL138AM, AND
9. Agree to use at least 1 highly effective method of contraception for the duration of study participation, and for 120 days after last dose of QXL138AM.
10. Male participants of child-bearing potential must:
11. Agree to use at least 1 highly effective method of contraception for the duration of study participation, and for 120 days after last dose of QXL138AM, AND
12. Refrain from sperm donation prior to the first dose of investigational product through 120 days following the last dose of QXL138AM.

Treatment Sites in Georgia